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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
Related Entities
Direct relations and traceable candidates grouped by relation type.
Candidate Herbs
target disease -> ingredient target -> herb ingredient8 Herbs
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