Endocrinology and Metabolism conditions, page 1 of 5
20 conditions on this page, alphabetically from Acquired night blindness to Glucosephosphate dehydrogenase deficiency. Each entry below describes the condition in full.
On this page
Acquired night blindness
acquired night blindness: A nutritional deficiency disease that is characterized by vitamin A deficiency causing poor adaptation of the eyes to low levels of light, and has_material_basis_in lack of vitamin A such that rhodopsin, a light sensitive retinal pigment, cannot be regenerated.
Classification
Ontology identifier: DOID:11491 (Human Disease Ontology).
Classification path: disease of metabolism › acquired metabolic disease › nutrition disease › nutritional deficiency disease.
Specialty: Endocrinology and Metabolism
Broader conditions
Medical codes
- ICD-10-CM: H53.62
- ICD-9-CM: 368.62
- SNOMED CT: 53808001
Care at Weyland-Yutani Health System
Endocrinology and Metabolism specialists lead care for acquired night blindness. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
Seek a medical evaluation if you are concerned about acquired night blindness. Bring a list of current medications and any previous test results.
Reference links
Adrenal cortex disease
adrenal cortex disease: An adrenal gland disease that is located_in the adrenal cortex.
Classification
Ontology identifier: DOID:3952 (Human Disease Ontology).
Classification path: disease of anatomical entity › endocrine system disease › adrenal gland disease.
Specialty: Endocrinology and Metabolism
Broader conditions
More specific conditions
Medical codes
- MeSH: D000303
- SNOMED CT: 129636003
Care at Weyland-Yutani Health System
Care for adrenal cortex disease is coordinated through Endocrinology and Metabolism. Your clinician will recommend tests and treatments based on your history and symptoms.
Treatment options
Diagnostic tests
When to seek care
If you or a family member may have adrenal cortex disease, contact your primary care provider or schedule a visit with Endocrinology and Metabolism.
Reference links
Adrenal gland disease
In clinical terms, adrenal gland disease is described as follows: an endocrine system disease that is located_in the adrenal gland.
Classification
Ontology identifier: DOID:9553 (Human Disease Ontology).
Classification path: disease of anatomical entity › endocrine system disease.
Specialty: Endocrinology and Metabolism
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: E27.9
- ICD-9-CM: 255.9
- MeSH: D000307
- SNOMED CT: 30171000
Care at Weyland-Yutani Health System
Treatment of adrenal gland disease begins with an evaluation in Endocrinology and Metabolism. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
When to seek care
Questions about adrenal gland disease? Call your nearest Weyland-Yutani location and ask for Endocrinology and Metabolism.
Reference links
Amino acid metabolic disorder
amino acid metabolic disorder: An inherited metabolic disorder that is characterized by impaired synthesis and degradation of amino acids.
Also known as
- inborn errors of amino acid metabolism
Classification
Ontology identifier: DOID:9252 (Human Disease Ontology).
Classification path: disease of metabolism › inherited metabolic disorder.
Specialty: Endocrinology and Metabolism
Broader conditions
More specific conditions
Medical codes
- MeSH: D000592
- SNOMED CT: 42930003
Care at Weyland-Yutani Health System
Endocrinology and Metabolism specialists lead care for amino acid metabolic disorder. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
Related articles
When to seek care
Seek a medical evaluation if you are concerned about amino acid metabolic disorder. Bring a list of current medications and any previous test results.
Reference links
Androgen insensitivity syndrome
A disorder of sexual development that is characterized by the inability of the cell to respond to androgens in individuals with a karyotype of 46,XY resulting in female physical traits but male genetic makeup. Our Endocrinology and Metabolism team evaluates and manages androgen insensitivity syndrome.
Also known as
- Androgen resistance syndrome
- Androgen-Insensitivity Syndrome
- Feminisation - testicular
- Goldberg - Maxwell syndrome
- Goldberg-Maxwell syndrome
- testicular feminization
- testicular Feminization syndrome
Classification
Ontology identifier: DOID:4674 (Human Disease Ontology).
Classification path: disease of anatomical entity › endocrine system disease › gonadal disease › disorder of sexual development.
Specialty: Endocrinology and Metabolism
Broader conditions
Medical codes
- ICD-10-CM: E34.5
- ICD-9-CM: 259.51
- MeSH: D013734
- OMIM: 300068
- SNOMED CT: 12313004
Care at Weyland-Yutani Health System
Endocrinology and Metabolism specialists lead care for androgen insensitivity syndrome. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
Seek a medical evaluation if you are concerned about androgen insensitivity syndrome. Bring a list of current medications and any previous test results.
Reference links
Calcinosis
A calcium metabolism disease that is the result of the formation of calcium deposits in any soft tissue. This page summarizes how calcinosis is classified and the care available at Weyland-Yutani Health System.
Also known as
- pathologic calcification
- Pathologically calcified structure
Classification
Ontology identifier: DOID:182 (Human Disease Ontology).
Classification path: disease of metabolism › acquired metabolic disease › mineral metabolism disease › calcium metabolism disease.
Specialty: Endocrinology and Metabolism
Broader conditions
More specific conditions
Medical codes
- MeSH: D002114
- SNOMED CT: 237881004
Care at Weyland-Yutani Health System
Care for calcinosis is coordinated through Endocrinology and Metabolism. Your clinician will recommend tests and treatments based on your history and symptoms.
Treatment options
Diagnostic tests
Related articles
When to seek care
Seek a medical evaluation if you are concerned about calcinosis. Bring a list of current medications and any previous test results.
Reference links
Carnitine-acylcarnitine translocase deficiency
Overview. A lipid metabolism disorder characterized by impaired long-chain fatty acid ozidation resulting in fasting-induced hypoketotic hypoglycemia, hyperammonemia, elevated creatine kinase and transaminases, dicarboxylic aciduria, very low free carnitine and abnormal acylcarnitine profile with marked elevation of the long-chain acylcarnitines that has_material_basis_in homozygous or compound heterozygous mutation in the SLC25A20 gene on chromosome 3p21.31. Weyland-Yutani Health System offers diagnosis and ongoing care for carnitine-acylcarnitine translocase deficiency.
Also known as
Classification
Ontology identifier: DOID:0111585 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal recessive disease.
Specialty: Endocrinology and Metabolism
Broader conditions
Medical codes
- MeSH: C562812
- OMIM: 212138
- SNOMED CT: 238003000
Care at Weyland-Yutani Health System
Care for carnitine-acylcarnitine translocase deficiency is coordinated through Endocrinology and Metabolism. Your clinician will recommend tests and treatments based on your history and symptoms.
Treatment options
Diagnostic tests
Related articles
When to seek care
Seek a medical evaluation if you are concerned about carnitine-acylcarnitine translocase deficiency. Bring a list of current medications and any previous test results.
Reference links
Copper deficiency myelopathy
In clinical terms, copper deficiency myelopathy is described as follows: A nutritional deficiency disease that is characterized by deficiency of copper, causing spastic gait and ataxia, often with anemia and neutropenia, has_symptom imbalance and jerking movements, and has_material_basis_in copper deficiency possibly due to malabsorption or excess zinc ingestion.
Also known as
Classification
Ontology identifier: DOID:5112 (Human Disease Ontology).
Classification path: disease of metabolism › acquired metabolic disease › nutrition disease › nutritional deficiency disease.
Specialty: Endocrinology and Metabolism
Broader conditions
Medical codes
- MeSH: D013540
- SNOMED CT: 78714004
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, copper deficiency myelopathy is managed by Endocrinology and Metabolism with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
When to seek care
Seek a medical evaluation if you are concerned about copper deficiency myelopathy. Bring a list of current medications and any previous test results.
Reference links
Corticosteroid-binding globulin deficiency
An adrenal gland disease characterized by decreased levels of serum corticosteroid-binding globulin and cortisol, and in some cases hypo- or hypertension, and muscle fatigue that has_material_basis_in heterozygous or homozygous mutation in the SERPINA6 gene on chromosome 14q32. This page summarizes how corticosteroid-binding globulin deficiency is classified and the care available at Weyland-Yutani Health System.
Also known as
- CBG deficiency
- transcortin deficiency
Classification
Ontology identifier: DOID:0090030 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease.
Specialty: Endocrinology and Metabolism
Broader conditions
Medical codes
- ICD-10-CM: E27.8
- MeSH: C565152
- OMIM: 611489
Care at Weyland-Yutani Health System
Endocrinology and Metabolism specialists lead care for corticosteroid-binding globulin deficiency. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
Seek a medical evaluation if you are concerned about corticosteroid-binding globulin deficiency. Bring a list of current medications and any previous test results.
Reference links
Diabetes mellitus
diabetes mellitus: A glucose metabolism disease that is characterized by chronic hyperglycaemia with disturbances of carbohydrate, fat and protein metabolism resulting from defects in insulin secretion, insulin action, or both.
Also known as
Classification
Ontology identifier: DOID:9351 (Human Disease Ontology).
Classification path: disease of metabolism › inherited metabolic disorder › carbohydrate metabolic disorder › glucose metabolism disease.
Specialty: Endocrinology and Metabolism
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: E08-E13
- ICD-9-CM: 250
- MeSH: D003920
- SNOMED CT: 267467004
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, diabetes mellitus is managed by Endocrinology and Metabolism with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
Related articles
When to seek care
Seek a medical evaluation if you are concerned about diabetes mellitus. Bring a list of current medications and any previous test results.
Reference links
Diabetic ketoacidosis
A metabolic acidosis that is characterized by the shift of acid-base status of the body toward the acid side accompanied by the accumulation of ketone bodies in body tissues and fluids, resulting from uncontrolled diabetes mellitus. This page summarizes how diabetic ketoacidosis is classified and the care available at Weyland-Yutani Health System.
Also known as
- DIABETES MELLITUS, KETOSIS-PRONE
- ketosis-prone diabetes mellitus
Classification
Ontology identifier: DOID:1837 (Human Disease Ontology).
Classification path: disease of metabolism › acquired metabolic disease › metabolic acidosis.
Specialty: Endocrinology and Metabolism
Broader conditions
Medical codes
- ICD-9-CM: 250.1
- MeSH: D016883
- OMIM: 612227
- SNOMED CT: 154671004
Care at Weyland-Yutani Health System
Endocrinology and Metabolism specialists lead care for diabetic ketoacidosis. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
Seek a medical evaluation if you are concerned about diabetic ketoacidosis. Bring a list of current medications and any previous test results.
Reference links
Disease of metabolism
A disease that involves errors in metabolic processes of building or degradation of molecules. This page summarizes how disease of metabolism is classified and the care available at Weyland-Yutani Health System.
Also known as
Classification
Ontology identifier: DOID:0014667 (Human Disease Ontology).
Specialty: Endocrinology and Metabolism
More specific conditions
Medical codes
- ICD-10-CM: E88.9
- ICD-9-CM: 277.9
- MeSH: D008659
- SNOMED CT: 75934005
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, disease of metabolism is managed by Endocrinology and Metabolism with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
Related articles
When to seek care
Seek a medical evaluation if you are concerned about disease of metabolism. Bring a list of current medications and any previous test results.
Reference links
Endemic goiter
endemic goiter: A nutritional deficiency disease characterized by noncancerous enlargement of the thyroid gland and has_material_basis_in iodine deficiency.
Also known as
- Iodine-deficiency-related endemic goitre
- simple goitre
Classification
Ontology identifier: DOID:13198 (Human Disease Ontology).
Classification path: disease of metabolism › acquired metabolic disease › nutrition disease › nutritional deficiency disease.
Specialty: Endocrinology and Metabolism
Broader conditions
Medical codes
- ICD-10-CM: E01.2
- ICD-9-CM: 240.0
- MeSH: D006043
- SNOMED CT: 271949009
Care at Weyland-Yutani Health System
Treatment of endemic goiter begins with an evaluation in Endocrinology and Metabolism. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
When to seek care
Questions about endemic goiter? Call your nearest Weyland-Yutani location and ask for Endocrinology and Metabolism.
Reference links
Endocrine pancreas disease
Overview. A pancreas disease that is located_in the endocrine component of the pancreas, consisting of islet cells (islets of Langerhans) that create and release important hormones directly into the bloodstream. Weyland-Yutani Health System offers diagnosis and ongoing care for endocrine pancreas disease.
Classification
Ontology identifier: DOID:1428 (Human Disease Ontology).
Classification path: disease of anatomical entity › endocrine system disease › pancreas disease.
Specialty: Endocrinology and Metabolism
Broader conditions
Medical codes
- ICD-10-CM: E16
- ICD-9-CM: 251
- SNOMED CT: 190427005
Care at Weyland-Yutani Health System
Care for endocrine pancreas disease is coordinated through Endocrinology and Metabolism. Your clinician will recommend tests and treatments based on your history and symptoms.
Treatment options
Diagnostic tests
When to seek care
If you or a family member may have endocrine pancreas disease, contact your primary care provider or schedule a visit with Endocrinology and Metabolism.
Reference links
Endocrine system disease
In clinical terms, endocrine system disease is described as follows: A disease of anatomical entity that is located_in endocrine glands which secretes a type of hormone directly into the bloodstream to regulate the body.
Classification
Ontology identifier: DOID:28 (Human Disease Ontology).
Classification path: disease of anatomical entity.
Specialty: Endocrinology and Metabolism
More specific conditions
Medical codes
- ICD-10-CM: E34.9
- ICD-9-CM: 259.9
- MeSH: D004700
- SNOMED CT: 67432001
Care at Weyland-Yutani Health System
Care for endocrine system disease is coordinated through Endocrinology and Metabolism. Your clinician will recommend tests and treatments based on your history and symptoms.
Treatment options
Diagnostic tests
When to seek care
If you or a family member may have endocrine system disease, contact your primary care provider or schedule a visit with Endocrinology and Metabolism.
Reference links
Eunuchism
Overview. A hypogonadism that is characterized by the lack of mature male germ cells and testicular hormones. Weyland-Yutani Health System offers diagnosis and ongoing care for eunuchism.
Classification
Ontology identifier: DOID:5003 (Human Disease Ontology).
Classification path: disease of anatomical entity › endocrine system disease › gonadal disease › hypogonadism.
Specialty: Endocrinology and Metabolism
Broader conditions
Medical codes
- MeSH: D005058
- SNOMED CT: 190559001
Care at Weyland-Yutani Health System
Endocrinology and Metabolism specialists lead care for eunuchism. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
Questions about eunuchism? Call your nearest Weyland-Yutani location and ask for Endocrinology and Metabolism.
Reference links
Familial hypocalciuric hypercalcemia 1
In clinical terms, familial hypocalciuric hypercalcemia 1 is described as follows: A familial hypocalciuric hypercalcemia that has_material_basis_in heterozygous loss-of-function mutations in the CASR gene on chromosome 3q21.
Also known as
- familial benign hypercalcemia 1
- familial hypocalciuric hypercalcemia type I
- FHH type 1
- HHC1
- hypocalciuric hypercalcemia type I
Classification
Ontology identifier: DOID:0060700 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal dominant disease › familial hypocalciuric hypercalcemia.
Specialty: Endocrinology and Metabolism
Broader conditions
Medical codes
- ICD-10-CM: E83.5
- OMIM: 145980
Care at Weyland-Yutani Health System
Care for familial hypocalciuric hypercalcemia 1 is coordinated through Endocrinology and Metabolism. Your clinician will recommend tests and treatments based on your history and symptoms.
Treatment options
Diagnostic tests
When to seek care
Seek a medical evaluation if you are concerned about familial hypocalciuric hypercalcemia 1. Bring a list of current medications and any previous test results.
Reference links
Favism
Overview. A glucosephosphate dehydrogenase deficiency characterized by a hemolytic reaction to consumption of broad beans. Weyland-Yutani Health System offers diagnosis and ongoing care for favism.
Classification
Ontology identifier: DOID:13628 (Human Disease Ontology).
Classification path: disease of metabolism › inherited metabolic disorder › carbohydrate metabolic disorder › glucosephosphate dehydrogenase deficiency.
Specialty: Endocrinology and Metabolism
Broader conditions
Medical codes
- ICD-10-CM: D55.0
- MeSH: D005236
- SNOMED CT: 154801000
Care at Weyland-Yutani Health System
Endocrinology and Metabolism specialists lead care for favism. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
Seek a medical evaluation if you are concerned about favism. Bring a list of current medications and any previous test results.
Reference links
Gestational diabetes
gestational diabetes: A diabetes mellitus that manifests during pregnancy.
Also known as
- GDM
- Gestational diabetes mellitus
- Maternal gestational diabetes mellitus
Classification
Ontology identifier: DOID:11714 (Human Disease Ontology).
Classification path: disease of metabolism › inherited metabolic disorder › carbohydrate metabolic disorder › glucose metabolism disease › diabetes mellitus.
Specialty: Endocrinology and Metabolism
Broader conditions
Medical codes
- ICD-10-CM: O24.4
- MeSH: D016640
- SNOMED CT: 11687002
Care at Weyland-Yutani Health System
Care for gestational diabetes is coordinated through Endocrinology and Metabolism. Your clinician will recommend tests and treatments based on your history and symptoms.
Treatment options
Diagnostic tests
Related articles
When to seek care
If you or a family member may have gestational diabetes, contact your primary care provider or schedule a visit with Endocrinology and Metabolism.
Reference links
Glucosephosphate dehydrogenase deficiency
glucosephosphate dehydrogenase deficiency: A carbohydrate metabolic disorder that is characterized by abnormally low levels of glucose-6-phosphate dehydrogenase (abbreviated G6PD or G6PDH).
Also known as
- deficiency of G-6PD
- Glucose-6-phosphate dehydrogenase deficiency
Classification
Ontology identifier: DOID:2862 (Human Disease Ontology).
Classification path: disease of metabolism › inherited metabolic disorder › carbohydrate metabolic disorder.
Specialty: Endocrinology and Metabolism
Broader conditions
More specific conditions
Medical codes
- MeSH: D005955
- SNOMED CT: 124134002
Care at Weyland-Yutani Health System
Treatment of glucosephosphate dehydrogenase deficiency begins with an evaluation in Endocrinology and Metabolism. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
When to seek care
Questions about glucosephosphate dehydrogenase deficiency? Call your nearest Weyland-Yutani location and ask for Endocrinology and Metabolism.
Reference links