01
Diseases
Deafness, Autosomal Recessive 88
deafness, autosomal recessive 88
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 2
Basic Information
Grouped by core information, identifiers, and descriptions.
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Core Information
- Disease Name
- Deafness, Autosomal Recessive 88
- Standard Disease Name
- deafness, autosomal recessive 88
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- D006222
- OMIM ID
- No data
- UMLS ID
- C0018552
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_NCI-GLOSS_1602D:A benign (not cancer) growth made up of an abnormal mixture of cells and tissues normally found in the area of the body where the growth occurs.|NCI2016_CDISC_1602D:An excessive but focal overgrowth of cells and tissues native to the organ in which it occurs.|NCI2016_02D:A benign and excessive tumor-like growth of mature cells and normal tissues which grow in a disorganized pattern.|MSH2017_2016_08_12:A focal malformation resembling a neoplasm, composed of an overgrowth of mature cells and tissues that normally occur in the affected area.|HPO2016_07_04:A disordered proliferation of mature tissues that is native to the site of origin - eg, exostoses, nevi and soft tissue hamartomas. Although most hamartomas are benign, some histologic subtypes - eg, neuromuscular hamartoma, may proliferate aggressively such as mesenchymal cystic hamartoma, Sclerosing epithelial hamartoma, Sclerosing metanephric hamartoma. [HPO:curators]
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