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Diseases

Schimke Immunoosseous Dysplasia

schimke immunoosseous dysplasia

Entity Type
Diseases
Relation Groups
3
Relation Preview
24

Basic Information

Grouped by core information, identifiers, and descriptions.

Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.

Core Information

Disease Name
Schimke Immunoosseous Dysplasia
Standard Disease Name
schimke immunoosseous dysplasia
MeSH Tree
No data
ICD-10
E31.0

Identifiers

DO ID
No data
MeSH ID
D016884
OMIM ID
No data
UMLS ID
C0085409
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:A rare genetic syndrome characterized by autoantibodies production against more than one endocrine organ. The range of endocrinopathies includes hypoparathyroidism, adrenal insufficiency, hypogonadism, type 1 diabetes mellitus and hypothyroidism.|MSH2017_2016_08_12:Autoimmune diseases affecting multiple endocrine organs. Type I is characterized by childhood onset and chronic mucocutaneous candidiasis (CANDIDIASIS, CHRONIC MUCOCUTANEOUS), while type II exhibits any combination of adrenal insufficiency (ADDISON'S DISEASE), lymphocytic thyroiditis (THYROIDITIS, AUTOIMMUNE;), HYPOPARATHYROIDISM; and gonadal failure. In both types organ-specific ANTIBODIES against a variety of ENDOCRINE GLANDS have been detected. The type II syndrome differs from type I in that it is associated with HLA-A1 and B8 haplotypes, onset is usually in adulthood, and candidiasis is not present.|CHV2011_02:an autoimmune diseases affecting multiple endocrine organs|CHV2011_02:an autoimmune diseases affecting multiple endocrine organs|CHV2011_02:an autoimmune diseases affecting multiple endocrine organs|CHV2011_02:an autoimmune diseases affecting multiple endocrine organs
Related

Direct relations and traceable candidates grouped by relation type.

Candidate Ingredients

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