clinic

Big Tree Medical Home

5 Stars (42 Reviews)

Big Tree Medical Home is a clinic that specializes in DPC Family Medicine and Concierge Pediatrics. The clinic is located in Columbia, Missouri. Big Tree Medical Home is known for housing expert physicians. Big Tree Medical Home offers all the services, treatments and procedures pertinent to the specialties mentioned above.

5 Doctors | Website
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About Big Tree Medical Home

"Big Tree saves you time and money by letting you take care of your health care on your own time and with the assistance of technology. It’s simple. It’s easy. It’s affordable. One monthly fee, unlimited care."

Address

200 Corporate Lake Drive Columbia,
MO 65203

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Adam Wheeler - 200 Corporate Lake Drive, Columbia, Missouri, 65203
Adam Wheeler, MD, MBA
Big Tree Medical Home
Concierge Pediatrics
(0)
Fee $0 - $0
Max no. of Patients: N/A
Accepting New Patients: NA
200 Corporate Lake Drive, Columbia, MO 65203
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Pavel Svintozelsky - 200 Corporate Lake Drive, Columbia, Missouri, 65203
Pavel Svintozelsky, MD
Big Tree Medical Home
DPC Family Medicine
(8)
Fee $0 - $0
Max no. of Patients: N/A
Accepting New Patients: NA
200 Corporate Lake Drive, Columbia, MO 65203
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Andrew Doppelt - 200 Corporate Lake Drive, Columbia, Missouri, 65203
Andrew Doppelt, MD
Big Tree Medical Home
DPC Family Medicine
(7)
Fee $0 - $0
Max no. of Patients: N/A
Accepting New Patients: NA
200 Corporate Lake Drive, Columbia, MO 65203
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Nathan Granneman - 200 Corporate Lake Drive, Columbia, Missouri, 65203
Nathan Granneman, MD
Big Tree Medical Home
DPC Family Medicine
(5)
Fee $0 - $0
Max no. of Patients: N/A
Accepting New Patients: NA
200 Corporate Lake Drive, Columbia, MO 65203
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Reviews
Posted by FMDD User
September 29, 2023

Review For Pavel Svintozelsky

Posted by FMDD User
January 05, 2024

Review For Pavel Svintozelsky

Posted by FMDD User
April 15, 2024
Enlightened me about my condition.

Review For Pavel Svintozelsky

Posted by FMDD User
March 01, 2024
Guided me in choosing the best treatment option.

Review For Pavel Svintozelsky

Conditions Treated
  • High blood pressure
  • High cholesterol
  • Congestive heart failure
  • Chronic fatigue syndrome
  • Cold urticaria
  • Comedones
  • Crooked teeth
  • Cyclic vomiting syndrome
  • Delayed ejaculation
  • Dermatitis herpetiformis
  • Diaphragmatic hernia
  • Digeorge syndrome
  • Diphallia
  • Dry eye
  • Ectodermal dysplasias
  • Encephalocele
  • Enlarged prostate
  • Epicanthal folds
  • Episcleritis
  • Epispadias
  • Esotropia
  • Exercise induced asthma
  • Farsightedness
  • Femoral hernia
  • Galactosemia
  • Gilbert syndrome
  • Glomerulonephritis
  • Granuloma annulare
  • Granulomatosis with polyangiitis
  • Grover's disease
  • Gum disease
  • Guttate psoriasis
  • Head lice
  • Henoch schonlein purpura
  • Horseshoe kidney
  • Liver disease
  • Hydrops fetalis
  • Hyperopia
  • Hypophosphatasia
  • Hypospadias
  • Iga nephropathy
  • Interstitial cystitis
  • Intertrigo
  • Intussusception
  • Juvenile dermatomyositis
  • Juvenile idiopathic arthritis
  • Kabuki syndrome
  • Keratitis
  • Keratoconus
  • Kidney disease
  • Krabbe disease
  • Kwashiorkor
  • Lazy eye
  • Lesch nyhan syndrome
  • Lichen sclerosis
  • Lichen simplex chronicus
  • Liver spots
  • Loose teeth
  • Low sodium level
  • Lungs
  • Male pattern baldness
  • Malignant hyperthermia
  • Maple syrup urine disease
  • Men's health
  • Meth addiction
  • Mittelschmerz
  • Mixed connective tissue disease
  • Mouth sores
  • Munchausen syndrome by proxy
  • Nephrotic syndrome
  • Pellagra
  • Pityriasis alba
  • Polymyalgia rheumatica
  • Gout
  • Congenital heart disease
  • Coronary artery disease
  • Coronary heart disease
  • Dextrocardia
  • Dilated cardiomyopathy
  • Ebstein's anomaly
  • Heart block
  • Heart disease
  • Hypoplastic left heart syndrome
  • Ischemic heart disease
  • Long qt syndrome
  • May thurner syndrome
  • Mitral regurgitation
  • Mitral valve prolapse
  • Mitral valve regurgitation
  • Noonan syndrome
  • Paroxysmal supraventricular tachycardia
  • Patent ductus arteriosus
  • Rheumatic fever
  • Situs inversus
  • Tetralogy of fallot
  • Truncus arteriosus
  • Vasoconstriction
  • Ventricular septal defects
  • Aphantasia
  • Apraxia
  • Cerebellar hypoplasia
  • Chronic headache
  • Dandy walker syndrome
  • Dravet syndrome
  • Duchenne muscular dystrophy
  • Erb's palsy
  • Essential tremor
  • Fragile x syndrome
  • Holoprosencephaly
  • Hydranencephaly
  • Hypotonia
  • Lennox gastaut syndrome
  • Lissencephaly
  • Microcephaly
  • Moebius syndrome
  • Myelomeningocele
  • Pompe disease
  • Rett syndrome
  • Spinal muscular atrophy
  • Sturge weber syndrome
  • Tuberous sclerosis
  • Acute flaccid myelitis
  • Adrenoleukodystrophy
  • Aicardi goutieres syndrome
  • Aicardi syndrome
  • Alexander disease
  • Encopresis
  • Esophageal atresia
  • Exocrine pancreatic insufficiency
  • Fecal impaction
  • Food allergy
  • Gastroesophageal reflux disease (gerd)
  • Hirschsprung disease
  • Inflammatory bowel disease
  • Lymphocytic colitis
  • Malabsorption
  • Necrotizing enterocolitis
  • Peptic ulcer
  • Peptic ulcer disease
  • Blount disease
  • Caudal regression syndrome
  • Clubfoot
  • De quervain's
  • Knock knees
  • Legg calve perthes disease
  • Osgood schlatter disease
  • Osteogenesis imperfecta
  • Pectus carinatum
  • Pectus excavatum
  • Polydactyly
  • Syndactyly
  • Burning mouth syndrome
  • Choanal atresia
  • Cholesteatoma
  • Chronic sinusitis
  • Dry mouth
  • Glossitis
  • Laryngomalacia
  • Microtia
  • Otitis
  • Otitis media
  • Acute otitis externa
  • Congenital adrenal hyperplasia
  • Diabetes insipidus
  • Diabetes mellitus
  • Gigantism
  • Growth hormone deficiency
  • Hashimoto thyroiditis
  • Hyperparathyroidism
  • Hypoparathyroidism
  • Low blood sugar
  • Magnesium deficiency
  • Phenylketonuria
  • Precocious puberty
  • Rickets
  • Albright's hereditary osteodystrophy
  • Candidiasis
  • Cat scratch disease
  • Chikungunya
  • Cholera
  • Dengue fever
  • Ehrlichiosis
  • Gingivostomatitis
  • Herpangina
  • Hiv aids
  • Influenza
  • Legionnaire disease
  • Leishmaniasis
  • Lemierre syndrome
  • Leptospirosis
  • Lymphogranuloma venereum
  • Melioidosis
  • Mumps
  • Noma
  • Parainfluenza
  • Pertussis
  • Rubella
  • Septicemia
  • Generalized anxiety disorder
  • Fanconi anemia
  • Hemolysis
  • Hemolytic anemia
  • Hemolytic uremic syndrome
  • Hemophilia a
  • Hermansky pudlak syndrome
  • Iron deficiency anemia
  • Leukocytosis
  • Purpura
  • Thalassemia
  • Castleman disease
  • Cherry angioma
  • Ewing sarcoma
  • Langerhans cell histiocytosis
  • Dermatitis
  • Atopic dermatitis
  • Eczema
  • Allergies
  • Sepsis
  • Hiatal hernia
  • Nausea
  • Hypertension
  • Seizures
  • Sarcoidosis
  • Diabetes
  • Cardiomyopathy
  • Arrhythmias
  • Menopause
  • Cystic fibrosis
  • Pneumonia
  • Inguinal hernia
  • Pulmonary embolism
  • Scleroderma
  • Tinea versicolor
  • Hemangioma
  • Asthma
  • Stroke
  • Acid reflux
  • Back pain
  • Multiple sclerosis
  • Sleep apnea
  • Gallstones
  • Lupus
  • Skin cancer
  • Melanoma
  • Canker sore
  • Pityriasis rosea
  • Vitiligo
  • Ear infection
  • Swimmer's ear
  • Hearing loss
  • Hypothyroidism
  • Hyperthyroidism
  • Muscle strains
  • Rotator cuff
  • Anal fissure
  • Psoriasis
  • Rosacea
  • Concussion
  • Cervical cancer
  • Insomnia
  • Eating disorders
  • Lactose intolerance
  • Celiac disease
  • Umbilical hernia
  • Deep vein thrombosis
  • Hydrocele
  • Rectal prolapse
  • Harlequin ichthyosis
  • Roseola
  • Depression
  • Irritable bowel syndrome
  • Ulcerative colitis
  • Hemorrhoids
  • Covid-19 testing
  • Tennis elbow
  • Cellulitis
  • Kawasaki disease
  • Diphtheria
  • Smallpox
  • Osteomyelitis
  • Measles
  • Meningitis
  • Molluscum contagiosum
  • Scurvy
  • Sjogren's syndrome
  • Narcolepsy
  • Strep throat
  • Kidney infection
  • Torticollis
  • Tension headache
  • Cerebral palsy
  • Restless legs syndrome
  • Strabismus
  • Milia
  • Testicular torsion
  • Hand-foot-and-mouth disease
  • Fifth disease
  • Tourette syndrome
  • Croup
  • Autism spectrum disorder
  • Asperger's syndrome
  • Scarlet fever
  • Upper respiratory infection
  • Adhd
  • Methemoglobinemia
  • Neuroblastoma
  • Newborn jaundice
  • Acute pharyngitis
  • Allergic conjunctivitis
  • Allergic cough
  • Allergic rhinitis
  • Anhidrosis
  • Aniridia
  • Bad breath
  • Beriberi
  • Black hairy tongue
  • Carbuncle
  • Chronic bronchitis
  • Chronic cough
  • Chronic illness
  • Chronic obstructive pulmonary disease
  • Primary care
  • Protein deficiency
  • Pulmonary fibrosis
  • Reye syndrome
  • Serum sickness
  • Superficial thrombophlebitis
  • Thrombophlebitis
  • Trimethylaminuria
  • Vitamin b12 deficiency
  • Central sleep apnea
  • Morning sickness
  • Add adhd
  • Anencephaly
  • Apert syndrome
  • Beckwith wiedemann syndrome
  • Brachydactyly
  • Cafe au lait spots
  • Cornelia de lange syndrome
  • Cri du chat syndrome
  • Crouzon syndrome
  • Cystinosis
  • Micrognathia
  • Pfeiffer syndrome
  • Poland syndrome
  • Progeria
  • Sotos syndrome
  • Stickler syndrome
  • Tay sachs disease
  • Treacher collins syndrome
  • Aarskog syndrome
  • Adams oliver syndrome
  • Adenosine deaminase deficiency
  • Caput succedaneum
  • Congenital diaphragmatic hernia
  • Cystic hygroma
  • Birthmarks
  • Craniosynostosis
  • Gastroschisis
  • Neonatal abstinence syndrome
  • Omphalocele
  • Plagiocephaly
  • Rhabdomyosarcoma
  • Selective mutism
  • Stork bite
  • Sudden infant death syndrome
  • Temper tantrums
  • Uncombable hair syndrome
  • Undescended testicle
  • Wilms tumor
  • Abo incompatibility
  • Acrodermatitis enteropathica
  • Cramps
  • Sore throat
  • Alopecia totalis
  • Alopecia universalis
  • Aphthous stomatitis
  • Aplasia cutis congenita
  • Barber say syndrome
  • Becker's nevus
  • Birt hogg dube syndrome
  • Bloom syndrome
  • Blue rubber bleb nevus syndrome
  • Bowenoid papulosis
  • Calcinosis
  • Candida infection of the skin
  • Cartilage hair hypoplasia
  • Chediak higashi syndrome
  • Cheilitis glandularis
  • Chromoblastomycosis
  • Cicatricial pemphigoid
  • Clear cell sarcoma
  • Cockayne syndrome
  • Corns and calluses
  • Creeping eruption
  • Cutaneous lupus erythematosus
  • Cutaneous t cell lymphoma
  • Cutis laxa
  • Cutis marmorata telangiectatica congenita
  • Dystrophic epidermolysis bullosa
  • Epidermolysis bullosa simplex
  • Gianotti crosti syndrome
  • Giant congenital melanocytic nevus
  • Hypohidrotic ectodermal dysplasia
  • Hypomelanosis of ito
  • Incontinentia pigmenti
  • Linear nevus sebaceous syndrome
  • Mongolian blue spots
  • Neonatal herpes
  • Netherton syndrome
  • Scalded skin syndrome
  • Aec syndrome
  • Baller gerold syndrome
  • Bannayan riley ruvalcaba syndrome
  • Bartsocas papas syndrome
  • Giant congenital nevus
  • Infantile digital fibromatosis
  • Infantile myofibromatosis
  • Junctional epidermolysis bullosa
  • Kerion celsi
  • Kindler syndrome
  • Megalencephaly capillary malformation syndrome
  • Meier gorlin syndrome
  • Perianal streptococcal cellulitis
  • Pik3ca related overgrowth spectrum
  • Pili torti
  • Pilonidal sinus disease
  • Pityriasis lichenoides et varioliformis acuta
  • Rothmund thomson syndrome
  • Scalp ear nipple syndrome
  • Sjogren larsson syndrome
  • Beare stevenson cutis gyrata syndrome
  • Cockayne syndrome type 2
  • Congenital generalized fibromatosis
  • Congenital herpes simplex
  • Cranioectodermal dysplasia
  • Curry jones syndrome
  • Farber lipogranulomatosis
  • Filippi syndrome
  • Gorlin chaudhry moss syndrome
  • Hemangioma thrombocytopenia syndrome
  • Nonbullous congenital ichthyosiform erythroderma
  • Phacomatosis pigmentokeratotica
  • Phacomatosis pigmentovascularis
  • Alstrom syndrome
  • Alternating hemiplegia of childhood
  • Amebiasis
  • Anaplastic large cell lymphoma
  • Anaplastic thyroid cancer
  • Angiodysplasia of the colon
  • Angioimmunoblastic t cell lymphoma
  • Anisakiasis
  • Annular pancreas
  • Annular tears
  • Anorectal abscess
  • Anti nmda receptor encephalitis
  • Antisynthetase syndrome
  • Anton syndrome
  • Aortic regurgitation
  • Aortic valve stenosis
  • Apnea of prematurity
  • Aquablation
  • Arachnodactyly
  • Arrhythmogenic right ventricular cardiomyopathy
  • Arterial embolism
  • Arterial insufficiency
  • Arthrogryposis multiplex congenita
  • Asymptomatic bacteriuria
  • Ataxia telangiectasia
  • Athetosis
  • Atrial myxoma
  • Atrioventricular septal defect
  • Atypical pneumonia
  • Atypical teratoid rhabdoid tumor
  • Auditory neuropathy spectrum disorder
  • Autosomal dominant polycystic kidney disease
  • Avian influenza
  • Axenfeld rieger syndrome
  • Axial spondyloarthritis
  • Bacterial food poisoning
  • Bacterial gastroenteritis
  • Bardet biedl syndrome
  • Barth syndrome
  • Bartter syndrome
  • Becker muscular dystrophy
  • Benign essential blepharospasm
  • Benign prostatic hypertrophy
  • Benign rolandic epilepsy
  • Bernard soulier syndrome
  • Biceps tendon rupture
  • Bilateral hydronephrosis
  • Bilateral perisylvian polymicrogyria
  • Bile acid malabsorption
  • Bile duct obstruction
  • Binder's syndrome
  • Biotinidase deficiency
  • Birdshot chorioretinopathy
  • Bladder outlet obstruction
  • Blau syndrome
  • Blepharophimosis
  • Blind loop syndrome
  • Bowel incontinence
  • Brachial plexopathy
  • Brain abscess
  • Brain herniation
  • Branchiootorenal syndrome
  • Breast cancer in men
  • Breast infection
  • Bronchial asthma
  • Bronchiolitis obliterans
  • Bronchogenic cyst
  • Bronchopulmonary dysplasia
  • Brown syndrome
  • Bulging fontanelles
  • Bursitis of the heel
  • Byssinosis
  • Campomelic dysplasia
  • Campylobacter infection
  • Canavan disease
  • Cancer pain
  • Capsule endoscopy
  • Cardiac amyloidosis
  • Carditis
  • Carney complex
  • Caroli disease
  • Carotid artery disease
  • Carotid stenosis
  • Carpenter syndrome
  • Cat eye syndrome
  • Cavernous sinus thrombosis
  • Central pain syndrome
  • Central serous chorioretinopathy
  • Cerebellar degeneration
  • Cerebral amyloid angiopathy
  • Cerebral cavernous malformation
  • Cerebral hypoxia
  • Cervical disc herniations
  • Cervical spinal stenosis
  • Cervical spine disorders
  • Char syndrome
  • Chemical pneumonitis
  • Cherubism
  • Chiari malformation type 2
  • Childhood disintegrative disorder
  • Chinese restaurant syndrome
  • Chondroblastoma
  • Chondrodysplasia
  • Chondroma
  • Chordoma
  • Choriocarcinoma
  • Choroid plexus cyst
  • Choroid plexus papilloma
  • Choroideremia
  • Chromophobe renal cell carcinoma
  • Chronic granulomatous disease
  • Chronic idiopathic constipation
  • Chronic inflammatory demyelinating polyneuropathy
  • Chronic myelogenous leukemia
  • Chronic myelomonocytic leukemia
  • Chronic renal disease
  • Chronic subdural hematoma
  • Chylous ascites
  • Claw foot
  • Cleft lip and palate
  • Cleft palate and cleft lip
  • Cloacal exstrophy
  • Cloudy cornea
  • Cmv retinitis
  • Coats disease
  • Coffin lowry syndrome
  • Coffin siris syndrome
  • Cogan's syndrome
  • Cohen syndrome
  • Cold and flu
  • Cold flu
  • Collagenous colitis
  • Coloboma of iris
  • Coloboma of optic nerve
  • Colorado tick fever
  • Cone rod dystrophy
  • Congenital cataract
  • Congenital generalized lipodystrophy
  • Congenital hyperinsulinism
  • Congenital hypothyroidism
  • Congenital lobar emphysema
  • Congenital myasthenic syndrome
  • Congenital syphilis
  • Congenital toxoplasmosis
  • Constrictive pericarditis
  • Cor triatriatum
  • Coronary artery spasm
  • Corpus callosum agenesis
  • Cortical dysplasia
  • Corticobasal degeneration
  • Costello syndrome
  • Cowden syndrome
  • Cramp fasciculation syndrome
  • Craniodiaphyseal dysplasia
  • Craniopharyngioma
  • Craniotabes
  • Crigler najjar syndrome
  • Crowded teeth
  • Cryptococcal meningitis
  • Infectious mononucleosis
  • Medication management
  • Meds
  • Arginase deficiency
  • Aspartylglucosaminuria
  • Beta ketothiolase deficiency
  • Idiopathic neutropenia
  • Lactate dehydrogenase deficiency
  • Secondary immunodeficiency
  • Beta mannosidosis
  • Cold induced sweating syndrome
  • Diffuse mesangial sclerosis
  • Ring chromosome 18
  • Short philtrum
  • Appendix cancer
  • Donnai barrow syndrome
  • Eec syndrome
  • Ellis van creveld syndrome
  • Emery dreifuss muscular dystrophy
  • Fanconi syndrome
  • Fetal hydantoin syndrome
  • Floating harbor syndrome
  • Foxg1 syndrome
  • Fraser syndrome
  • Freeman sheldon syndrome
  • Frontonasal dysplasia
  • Fumarase deficiency
  • Glucose 6 phosphate dehydrogenase deficiency
  • Glutaric acidemia type 1
  • Gm1 gangliosidosis
  • Hallermann streiff syndrome
  • Hemihyperplasia
  • Heterotaxy syndrome
  • Holt oram syndrome
  • Hypochondroplasia
  • Jacobsen syndrome
  • Koolen de vries syndrome
  • Lowe syndrome
  • Menkes disease
  • Menkes syndrome
  • Miller dieker syndrome
  • Miller syndrome
  • Muenke syndrome
  • Myotonia congenita
  • Nail patella syndrome
  • Nemaline myopathy
  • Nephronophthisis
  • Neuronal ceroid lipofuscinoses
  • Niemann pick disease
  • Pierre robin sequence
  • Pitt hopkins syndrome
  • Potocki lupski syndrome
  • Propionic acidemia
  • Roberts syndrome
  • Robinow syndrome
  • Rubinstein taybi syndrome
  • Saethre chotzen syndrome
  • Seckel syndrome
  • Single palmar crease
  • Sirenomelia
  • Smith lemli opitz syndrome
  • Smith magenis syndrome
  • Spondyloepiphyseal dysplasia
  • Tetrasomy x
  • Thanatophoric dysplasia
  • Triple x syndrome
  • Trisomy 14 mosaicism
  • Vacterl association
  • Von gierke disease
  • Wagr syndrome
  • Weaver syndrome
  • Wiedemann steiner syndrome
  • Zellweger syndrome
  • Acalvaria
  • Achondrogenesis
  • Acrodysostosis
  • Adenylosuccinate lyase deficiency
  • Allan herndon dudley syndrome
  • Alpers huttenlocher syndrome
  • Alpha mannosidosis
  • Andersen disease
  • Argininosuccinic aciduria
  • Arterial tortuosity syndrome
  • Asphyxiating thoracic dystrophy
  • Behr syndrome
  • Chromosome 22 duplication
  • Chromosome 8p deletion
  • Classic galactosemia
  • Dubowitz syndrome
  • Fanconi bickel syndrome
  • Feingold syndrome
  • Femoral facial syndrome
  • Fetal cystic hygroma
  • Fg syndrome
  • Fryns syndrome
  • Fucosidosis
  • Gaba transaminase deficiency
  • Galactokinase deficiency
  • Galactosialidosis
  • Galloway mowat syndrome
  • Gangliosidosis
  • Gaucher disease type 2
  • Gaucher disease type 3
  • Geleophysic dysplasia
  • Glutaric acidemia type 2
  • Hennekam syndrome
  • Holocarboxylase synthetase deficiency
  • Icf syndrome
  • Isovaleric acidemia
  • Jackson weiss syndrome
  • Johanson blizzard syndrome
  • Kaufman oculocerebrofacial syndrome
  • Kniest dysplasia
  • Knobloch syndrome
  • L1 syndrome
  • Lambdoid synostosis
  • Langer mesomelic dysplasia
  • Leri weill dyschondrosteosis
  • Mandibuloacral dysplasia
  • Marden walker syndrome
  • Marinesco sjogren syndrome
  • Marshall smith syndrome
  • Marshall syndrome
  • Mass phenotype
  • Mckusick kaufman syndrome
  • Meckel syndrome
  • Medium chain acyl coa dehydrogenase deficiency
  • Mosaic trisomy 7
  • Mosaic trisomy 8
  • Mosaic trisomy 9
  • Mucolipidosis type 4
  • Mucopolysaccharidosis type 1
  • Mucopolysaccharidosis type 2
  • Mucopolysaccharidosis type 3
  • Myhre syndrome
  • Nicolaides baraitser syndrome
  • Nijmegen breakage syndrome
  • Ohdo syndrome
  • Opitz g bbb syndrome
  • Pallister hall syndrome
  • Pallister killian mosaic syndrome
  • Peho syndrome
  • Pentasomy x
  • Perlman syndrome
  • Peters plus syndrome
  • Popliteal pterygium syndrome
  • Prekallikrein deficiency
  • Primary carnitine deficiency
  • Progressive myoclonic epilepsy
  • Pyridoxine deficiency
  • Pyruvate carboxylase deficiency
  • Rapadilino syndrome
  • Renpenning syndrome
  • Russell silver dwarfism
  • Schimke immuno osseous dysplasia
  • Schindler disease
  • Schinzel giedion syndrome
  • Schwartz jampel syndrome
  • Sea blue histiocytosis
  • Severe congenital neutropenia
  • Short chain acyl coa dehydrogenase deficiency
  • Short qt syndrome
  • Short syndrome
  • Sialidosis
  • Simpson golabi behmel syndrome
  • Smith kingsmore syndrome
  • Snyder robinson syndrome
  • Spinal muscular atrophy type 2
  • Spinal muscular atrophy type 3
  • Spondylocostal dysostosis
  • Spondyloepiphyseal dysplasia congenita
  • Stuve wiedemann syndrome
  • Temple syndrome
  • Tetra amelia syndrome
  • Tetrasomy 9p
  • Thrombocytopenia absent radius syndrome
  • Townes brocks syndrome
  • Trisomy 2 mosaicism
  • Van maldergem syndrome
  • Vici syndrome
  • Wiedemann rautenstrauch syndrome
  • Anophthalmia plus syndrome
  • Ballinger wallace syndrome
  • Benign familial neonatal seizures
  • Bowen conradi syndrome
  • C syndrome
  • Carey fineman ziter syndrome
  • Charlie m syndrome
  • Cln1 disease
  • Cln3 disease
  • Cln5 disease
  • Coloboma of eye lens
  • Congenital afibrinogenemia
  • Congenital aplastic anemia
  • Congenital fibrinogen deficiency
  • Congenital hemolytic anemia
  • Congenital lipoid adrenal hyperplasia
  • Congenital microcoria
  • Congenital plasminogen deficiency
  • Craniofacial deafness hand syndrome
  • Cytochrome p450 oxidoreductase deficiency
  • Dehydrated hereditary stomatocytosis
  • Desbuquois syndrome
  • Dihydropteridine reductase deficiency
  • Distal 18q deletion syndrome
  • Encephalocele anencephaly
  • Familial glucocorticoid deficiency
  • Familial hypopituitarism
  • Familial paroxysmal nonkinesigenic dyskinesia
  • Familial porencephaly
  • Fetal akinesia sequence
  • Fetal thalidomide syndrome
  • Fountain syndrome
  • Frank ter haar syndrome
  • Galactose epimerase deficiency
  • Gemss syndrome
  • Genetic epilepsy with febrile seizures plus
  • Genital dwarfism
  • Hardikar syndrome
  • Hemophilia a or b
  • Histidinemia
  • Homocystinuria due to mthfr deficiency
  • Hyperlysinemia
  • Hypochondrogenesis
  • Inborn amino acid metabolism disorder
  • Increased head circumference
  • Microcephalic osteodysplastic primordial dwarfism type 1
  • Microcephalic osteodysplastic primordial dwarfism type 2
  • Mucolipidosis 3
  • Mucopolysaccharidosis type 3a
  • Mucopolysaccharidosis type 3b
  • Mucopolysaccharidosis type 4
  • Mucopolysaccharidosis type 4a
  • Mucopolysaccharidosis type 6
  • Mucopolysaccharidosis type 7
  • Mulibrey nanism
  • Ornithine translocase deficiency
  • Orofaciodigital syndrome 1
  • Orotic aciduria type 1
  • Overhydrated hereditary stomatocytosis
  • Pena shokeir syndrome type 2
  • Peroxisomal acyl coa oxidase deficiency
  • Pgm1 cdg
  • Phosphoglycerate kinase deficiency
  • Phosphoglycerate mutase deficiency
  • Pmm2 congenital disorder of glycosylation
  • Potassium aggravated myotonia
  • Toriello carey syndrome
  • Trisomy 12 mosaicism
  • Trisomy 17 mosaicism
  • Trisomy 3 mosaicism
  • Walker dyson syndrome
  • X linked creatine deficiency
  • X linked infantile spinal muscular atrophy
  • X linked intellectual disability
  • X linked severe combined immunodeficiency
  • Yunis varon syndrome
  • Nephrogenic diabetes insipidus
  • Newborn low blood sugar
  • Pituitary dwarfism
  • Short stature
  • Delayed growth
  • Neonatal hypothyroidism
  • Pediatric obesity
  • Pinealectomy
  • Puberty disorder
  • Childhood hypophosphatasia
  • Hereditary hypophosphatemic rickets
  • Infant hyperglycemia
  • Isolated growth hormone deficiency
  • Neonatal severe hyperparathyroidism
  • Transient neonatal diabetes mellitus
  • Hemimegalencephaly
  • Infant botulism
  • Juvenile myoclonic epilepsy
  • Landau kleffner syndrome
  • Myoclonic epilepsy
  • Periventricular leukomalacia
  • Polymicrogyria
  • Pontocerebellar hypoplasia
  • Porencephaly
  • Rasmussen encephalitis
  • Spinal muscular atrophy type 1
  • West syndrome
  • Acute cerebellar ataxia
  • Bilirubin encephalopathy
  • Congenital mirror movement disorder
  • Diencephalic syndrome
  • Door syndrome
  • Dopa responsive dystonia
  • Early infantile epileptic encephalopathy
  • Intraventricular hemorrhage of the newborn
  • Marcus gunn phenomenon
  • Opsoclonus myoclonus syndrome
  • Periventricular heterotopia
  • Post traumatic epilepsy
  • Primary amebic meningoencephalitis
  • Satoyoshi syndrome
  • Congenital fiber type disproportion
  • Congenital muscular dystrophy type 1a
  • Cytoplasmic body myopathy
  • Epilepsy with myoclonic atonic seizures
  • Horizontal gaze palsy with progressive scoliosis
  • Hydrocephalus due to congenital stenosis of aqueduct of sylvius
  • Infantile onset spinocerebellar ataxia
  • Oculocerebrocutaneous syndrome
  • Oppenheim dystonia
  • Cytomegalovirus infection
  • Meningococcemia
  • Neonatal conjunctivitis
  • Neonatal sepsis
  • Torch syndrome
  • Toxocariasis
  • Congenital cytomegalovirus
  • Cytomegalic inclusion disease
  • H influenzae meningitis
  • Visceral larva migrans
  • Congenital mumps
  • Cryptosporidium enteritis
  • Rubella or measles
  • Duodenal atresia
  • Hepatoblastoma
  • Imperforate anus
  • Infantile pyloric stenosis
  • Tracheoesophageal fistula
  • Childhood pancreatitis
  • Colonic atresia
  • Congenital hepatic fibrosis
  • Congenital sucrase isomaltase deficiency
  • Gastroesophageal reflux in infants
  • Intestinal pseudo obstruction
  • Neonatal hemochromatosis
  • Atresia of small intestine
  • Berdon syndrome
  • Congenital nonhemolytic jaundice
  • Omphalomesenteric cyst
  • Primary intestinal lymphangiectasia
  • Cyclic neutropenia
  • Hemolytic disease of the newborn
  • Hemophagocytic lymphohistiocytosis
  • Hereditary spherocytosis
  • Juvenile myelomonocytic leukemia
  • Platelet storage pool deficiency
  • Childhood acute myeloid leukemia
  • Ganglioneuroma
  • Rhabdoid tumor
  • Rhabdomyosarcoma embryonal
  • Congenital mesoblastic nephroma
  • Embryonal tumor with multilayered rosettes
  • Ganglioneuroblastoma
  • Pediatric brain tumors
  • Pleuropulmonary blastoma
  • Primitive neuroectodermal tumor
  • Kohler disease
  • Slipped capital femoral epiphysis
  • Sprengel deformity
  • Congenital radioulnar synostosis
  • Congenital contractures
  • Congenital femoral deficiency
  • Stereotypic movement disorder
  • Transient tic disorder
  • Peer relationships
  • Developmental expressive language disorder
  • Developmental reading disorder
  • Pfapa
  • Toxic synovitis
  • Juvenile temporal arteritis
  • Neonatal onset multisystem inflammatory disease
  • Eisenmenger syndrome
  • Grass allergy
  • Meconium aspiration syndrome
  • Newborn transient tachypnea
  • Pulmonary atresia
  • Tracheobronchomalacia
  • Acute bronchiolitis
  • Congenital central hypoventilation syndrome
  • Congenital tracheomalacia
  • Idiopathic pulmonary hemosiderosis
  • Infantile apnea
  • Lung agenesis
  • Congenital pulmonary lymphangiectasia
  • Cystic adenomatoid malformation of lung
  • Endocardial cushion defect
  • Interrupted aortic arch
  • Pulmonary valve stenosis
  • Supravalvular aortic stenosis
  • Total anomalous pulmonary venous return
  • Transposition of the great arteries
  • Tricuspid atresia
  • Aortopulmonary window
  • Congenital anomalies of the heart
  • Congenital heart block
  • Double outlet left ventricle
  • Endocardial fibroelastosis
  • Mitral atresia
  • Pediatric myocarditis
  • Pulmonary atresia with intact ventricular septum
  • Right ventricle hypoplasia
  • Sternal cleft
  • Subvalvular aortic stenosis
  • Anomalous left coronary artery from the pulmonary artery
  • Arterial calcification of infancy
  • Congenital mitral stenosis
  • Fetal edema
  • High blood pressure in infants
  • Partial atrioventricular canal
  • Pulmonary atresia with ventricular septal defect
  • Ear tag
  • Metopic ridge
  • Penoscrotal transposition
  • Arrhinia
  • Exstrophy epispadias complex
  • Palatopharyngeal incompetence
  • Enlarged adenoids
  • Evans syndrome
  • Exstrophy of the bladder
  • Hemophilia b
  • Laryngeal cleft
  • Meatal stenosis
  • Meningocele
  • Nasal flaring
  • Otitis media with effusion
  • Potter syndrome
  • Prune belly syndrome
  • Retinopathy of prematurity
  • Severe combined immunodeficiency
  • Small for gestational age
  • Sunken fontanelles
  • Twin to twin transfusion syndrome
  • Velopharyngeal insufficiency
  • Aural polyps
  • Congenital nephrotic syndrome
  • Duplication of urethra
  • Infant hearing loss
  • Newborn head molding
  • Newborn polycythemia
  • Paroxysmal cold hemoglobinuria
  • Premature infant
  • Tracheal agenesis
  • Transient erythroblastopenia of childhood
  • Visceromegaly
  • And breastfeeding
  • Asphyxia neonatorum
  • Childhood iron deficiency anemia
  • Childhood volvulus
  • Fetal and neonatal alloimmune thrombocytopenia
  • Hygroma cervical
  • Neonatal ovarian cyst
  • Paris trousseau thrombocytopenia
  • Ulcers
  • Primary immunodeficiency
  • Monkeypox
  • Hmpv virus
more..
Treatments & Procedures
  • Blood pressure medication
  • Allergy testing
  • Ear tubes
  • Ear wax removal
  • Lumbar puncture
  • Dexa scan
  • Physical examination
  • Well child visits
  • Blood glucose monitoring
  • Bone density test
  • Cancer screening
  • Annual wellness exam
  • Chronic care management
  • Care coordination
  • Blood tests
  • Clinical trials
  • Smoking cessation
  • Staple removal
  • Vaccines
  • Immunizations
  • X ray
  • Pediatric urgent care
  • Immunization
  • Circumcision
  • Medical ear piercing
  • Tetralogy of fallot repair
  • Tof repair
  • Prematurity and low birth weight
  • Dental exams and cleanings
  • Pediatric laproscopy
  • Pediatric thoracoscopy
  • Pediatric sleep problems
  • Semaglutide
more..
Additional Services
  • Weight Loss

Frequently Asked Questions

Where is Big Tree Medical Home located?

Big Tree Medical Home is located in 200 Corporate Lake Drive Columbia, MO 65203.

What are the various modes of payment does Big Tree Medical Home Accept?

Big Tree Medical Home accepts Card | Cash.

What are the doctors who practice in Big Tree Medical Home specialize in?

Currently there are around 4 providers practice in Big Tree Medical Home who specialise in DPC Family Medicine and Concierge Pediatrics, etc

How can I make appointments with doctors in Big Tree Medical Home?

You can take appointments for doctors who practice in Big Tree Medical Home online on their website or by calling them.

Location
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