Hypotrichosis 15
Disease ID: disease_node_14209
Connections displayed (default: 10).
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| Dbxref | MIM:620177 |
|---|---|
| Subclassof | DOID_4535, DOID_0050737 |
| Data Source | DOID |
| Doid Label | hypotrichosis 15 |
| Doid Description | A hypotrichosis that is characterized by sparse or absent hair on the scalp and/or body, and eyebrows and eyelashes may be sparse or absent as well that has_material_basis_in homozygous mutation in the C3ORF52 gene on chromosome 3q13. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_14209 |
| Doid Id | DOID_0060968 |
| Label | Hypotrichosis 15 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Hypotrichosis(ID:disease_node_4232) (Disease)