Monilethrix
Disease ID: disease_node_12277
Connections displayed (default: 10).
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| Dbxref | GARD:93, ICD10CM:Q84.1, MESH:D056734, MIM:158000, NCI:C84894, SNOMEDCT_US_2023_03_01:69488000, UMLS_CUI:C0546966 |
|---|---|
| Subclassof | DOID_0050736, DOID_421 |
| Data Source | DOID, MESH |
| Mesh Id | D056734 |
| Mesh Label | Monilethrix |
| Mesh Subclassof | D006201, D000015, D012873 |
| Doid Label | monilethrix |
| Doid Description | A hair disease that is characterized by short, easily broken hair that results in alopecia and has_material_basis_in mutations in genes for type II hair cortex keratins. OMIM mapping confirmed by DO. [SN]. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_12277 |
| Doid Id | DOID_0050472 |
| Label | Monilethrix |
- Outgoing r'ship
SUBCLASS_OFto/from Hair Diseases(ID:disease_node_3643) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)