clinic

Ethos Endocrinology - Houston, Texas

5 Stars (10 Reviews)

Ethos Endocrinology is a clinic in Houston, TX offering Concierge Endocrinology, with 1 physician on staff.

1 Doctor | Website
Overview
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About Ethos Endocrinology

"Ethos Endocrinology restores the sacred bond of the patient-doctor relationship. We do that by employing a direct care model.After completing his residency and fellowship training at the highly-ranked Baylor College of Medicine in the Texas Medical Center, Dr. Kanji designed a health care experience to restore the patient-doctor relationship. How?

First, eliminate interference from insurance. Second, limit the number of members to maximize your time and experience. Third, keep it affordable. The result is Ethos Endocrinology."

Address

2500 Fondren Road Suite 320, Houston,
TX 77085

Modes of Payment

Card | Cash

Providers
Aleem Kanji - 2500 Fondren Road, Houston, Texas, 77085
Aleem Kanji, MD
Ethos Endocrinology
Concierge Endocrinology
(10)
Fee $101 - $250
Max no. of Patients: N/A
Accepting New Patients: NA
2500 Fondren Road, Suite 320, Houston, TX 77085
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Conditions Treated
  • Ectopic pregnancy
  • Osteoporosis
  • Obesity
  • Type 2 diabetes
  • Diabetes
  • Atherosclerosis
  • Diabetic ketoacidosis
  • Thyroid cancer
  • Adenomyosis
  • Endometriosis
  • Thyroid eye disease
  • Uterine fibroids
  • Hypothyroidism
  • Hyperthyroidism
  • Type 1 diabetes
  • Cushing syndrome
  • Ovarian cysts
  • Graves' disease
  • Gestational diabetes
  • Diabetic neuropathy
  • Metabolic syndrome
  • Noonan syndrome
  • Hypopituitarism
  • Pituitary tumor
  • Prolactinoma
  • Carcinoid syndrome
  • Malnutrition
  • Neuroendocrine tumor
  • Non alcoholic fatty liver disease
  • Zollinger ellison syndrome
  • Abetalipoproteinemia
  • Acromegaly
  • Androgen insensitivity syndrome
  • Apoplexy
  • Congenital adrenal hyperplasia
  • Diabetes insipidus
  • Diabetes mellitus
  • Diabetic foot ulcers
  • Diabetic retinopathy
  • Gigantism
  • Growth hormone deficiency
  • High potassium level
  • Hyperaldosteronism
  • Hypercalcemia
  • Hyperparathyroidism
  • Hypogonadism
  • Hypoparathyroidism
  • Hypophosphatemia
  • Kallmann syndrome
  • Low blood sugar
  • Low testosterone
  • Macrosomia
  • Magnesium deficiency
  • Metabolic acidosis
  • Osteomalacia
  • Papillary thyroid cancer
  • Phenylketonuria
  • Pheochromocytoma
  • Precocious puberty
  • Rickets
  • Thyroid nodule
  • Thyroid storm
  • Thyroiditis
  • Xanthoma
  • Adrenal cancer
  • Adrenal gland adenoma
  • Adrenocortical carcinoma
  • Albright's hereditary osteodystrophy
  • Alcoholic ketoacidosis
  • Follicular cyst of the ovary
  • Pituitary dwarfism
  • Premature ovarian failure
  • Diabetic foot care
  • Diabetic macular edema
  • Diabetic nephropathy
  • Diabetic peripheral neuropathy
  • Empty sella syndrome
  • Alstrom syndrome
  • Anaplastic thyroid cancer
  • Bardet biedl syndrome
  • Bartter syndrome
  • Congenital hyperinsulinism
  • Congenital hypothyroidism
  • Follicular thyroid cancer
  • Glucagonoma
  • Hypoaldosteronism
  • Hypogonadotropic hypogonadism
  • Low potassium level
  • Insulinoma
  • Liddle syndrome
  • Male infertility
  • Multiple endocrine neoplasia
  • Medullary thyroid carcinoma
  • Milk alkali syndrome
  • Nephrocalcinosis
  • Nephrogenic diabetes insipidus
  • Newborn low blood sugar
  • Parathyroid adenoma
  • Parathyroid cancer
  • Pituitary apoplexy
  • Pseudohypoparathyroidism
  • Renal glycosuria
  • Short stature
  • Multiple endocrine neoplasia type 2
  • Subacute thyroiditis
  • Thyroid disorders
  • Weight management
  • Acute adrenal crisis
  • Breast enlargement in males
  • Delayed growth
  • Nelson syndrome
  • Ectopic cushing syndrome
  • Endocrinology and metabolism
  • Exogenous cushing syndrome
  • Hypoglycemic coma
  • Hypothalamic tumor
  • Idiopathic hypercalciuria
  • Neonatal hypothyroidism
  • Non toxic goiter
  • Osteitis fibrosa
  • Ovarian dysfunction
  • Parathyroid hyperplasia
  • Pediatric obesity
  • Pinealectomy
  • Progressive osseous heteroplasia
  • Puberty disorder
  • Somatostatinoma
  • Testicular failure
  • Thyrotoxic periodic paralysis
  • Benign thyroid diseases
  • Childhood hypophosphatasia
  • Cushing syndrome due to adrenal tumor
  • Familial hypertension
  • Panhypopituitarism
  • Fertility and conception
  • Hereditary hypophosphatemic rickets
  • Hyperlipidemia type 3
  • Hyperlipoproteinemia type 4
  • Hypervitaminosis d
  • Mccune albright syndrome
  • Familial partial lipodystrophy
  • Shapiro syndrome
  • Secondary adrenal insufficiency
  • Syndrome of inappropriate antidiuretic hormone secretion
  • Apparent mineralocorticoid excess
  • Autoimmune polyglandular syndrome type 2
  • Maturity onset diabetes of the young
  • Overweight and obesity
  • Primary angle closure glaucoma
  • Pseudohypoaldosteronism type 1
  • Rabson mendenhall syndrome
  • Silent thyroiditis
  • Toxic nodular goiter
  • Abdominal obesity metabolic syndrome
  • Diabetic hyperglycemic hyperosmolar syndrome
  • Diabetic kidney disorder
  • Familial isolated hyperparathyroidism
  • Generalized resistance to thyroid hormone
  • Granulomatous hypophysitis
  • Floating harbor syndrome
  • Gitelman syndrome
  • Gonadal dysgenesis
  • Laron syndrome
  • Ornithine transcarbamylase deficiency
  • Swyer syndrome
  • Wolfram syndrome
  • Aromatase deficiency
  • Disorders of lipoid metabolism
  • Familial combined hyperlipidemia
  • Familial hypertriglyceridemia
  • Familial hypobetalipoproteinemia
  • Fanconi bickel syndrome
  • Female infertility
  • Galactokinase deficiency
  • Glucocorticoid remediable aldosteronism
  • Glucocorticoid resistance
  • Glycogen storage disease type 0
  • Glycogen storage disease type 3
  • Heterozygous familial hypercholesterolemia
  • Homozygous familial hypercholesterolemia
  • Leydig cell hypoplasia
  • Molybdenum cofactor deficiency
  • Multiple symmetric lipomatosis
  • Partial androgen insensitivity syndrome
  • Persistent mullerian duct syndrome
  • Pyruvate dehydrogenase deficiency
  • Russell silver dwarfism
  • Short chain acyl coa dehydrogenase deficiency
  • Short syndrome
  • Sitosterolemia
  • Thyroid dysgenesis
  • Triple a syndrome
  • Very long chain acyl coa dehydrogenase deficiency
  • Wolcott rallison syndrome
  • Acromegaloid facial appearance syndrome
  • Autosomal dominant hypocalcemia
  • Carnitine palmitoyltransferase 1 deficiency
  • Congenital lipoid adrenal hyperplasia
  • Cytochrome p450 oxidoreductase deficiency
  • Essential pentosuria
  • Familial glucocorticoid deficiency
  • Familial hdl deficiency
  • Familial hyperaldosteronism
  • Familial hypopituitarism
  • Familial lipoprotein lipase deficiency
  • Fructose 1
  • Genital dwarfism
  • Glucose transporter deficiency
  • Hereditary paraganglioma pheochromocytoma syndrome
  • Hyperglycerolemia
  • Hypolipoproteinemia
  • Infant hyperglycemia
  • Isolated growth hormone deficiency
  • Menopausal and postmenopausal disorders
  • Metastatic insulinoma
  • Neonatal severe hyperparathyroidism
  • Neurohypophyseal diabetes insipidus
  • Osteoporosis pseudoglioma syndrome
  • Ovarian overproduction of androgens
  • Transient neonatal diabetes mellitus
  • Weight control and obesity
  • Isolated acth deficiency
  • Isolated hypogonadotropic hypogonadism
  • Kenny caffey syndrome type 2
  • Long chain 3 hydroxyacyl coa dehydrogenase deficiency
  • Malonyl coa decarboxylase deficiency
  • Maternal hyperphenylalaninemia
  • Methylmalonic acidemia with homocystinuria
  • Morgagni stewart morel syndrome
  • Multiple carboxylase deficiency
  • Ornithine translocase deficiency
  • Peroxisomal acyl coa oxidase deficiency
  • Pgm1 cdg
  • Pmm2 congenital disorder of glycosylation
  • Rft1 cdg
  • Thyroid hormone plasma membrane transport defect
  • Type a insulin resistance syndrome
  • Type b insulin resistance syndrome
  • Hyperlipoproteinemia type 5
  • Pseudohypoaldosteronism type 2
  • Fibrous dysplasia
  • Hashimoto thyroiditis
  • Ovarian hyperstimulation syndrome
  • Alkaptonuria
  • Female pattern baldness
  • Hirsutism in women
  • Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy
  • Cold induced sweating syndrome
  • Donohue syndrome
  • Multiple endocrine neoplasia type 1
  • Carnitine acylcarnitine translocase deficiency
  • Addison's disease
  • Polycystic ovarian syndrome (pcos)
  • Familial hypercholesterolemia
more..
Treatments & Procedures
  • Hormone replacement therapy
  • Dexa scan
  • Bone density test
  • Blood glucose monitoring
  • Insulin treatment
  • Bone densitometry
  • Hormone treatments
  • Dietary counseling
  • Pcos
  • Point of care a1c

Frequently Asked Questions

Where is Ethos Endocrinology located?

Ethos Endocrinology is located in 2500 Fondren Road Suite 320, Houston, TX 77085.

What are the various modes of payment does Ethos Endocrinology Accept?

Ethos Endocrinology accepts Card | Cash.

What are the doctors who practice in Ethos Endocrinology specialize in?

Currently there are around 1 providers practice in Ethos Endocrinology who specialise in Concierge Endocrinology, etc

How can I make appointments with doctors in Ethos Endocrinology?

You can take appointments for doctors who practice in Ethos Endocrinology online on their website or by calling them.

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