Primary Autosomal Domit Microcephaly 18
Disease ID: disease_node_19305
Connections displayed (default: 10).
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| Dbxref | MIM:617520 |
|---|---|
| Subclassof | DOID_0050736, DOID_0070297 |
| Data Source | DOID |
| Synonyms | MCPH18 |
| Doid Label | primary autosomal domit microcephaly 18 |
| Doid Description | A primary microcephaly that has_material_basis_in heterozygous mutation in the WDFY3 gene on chromosome 4q21. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_19305 |
| Doid Id | DOID_0070295 |
| Label | Primary Autosomal Domit Microcephaly 18 |
- Outgoing r'ship
SUBCLASS_OFto/from Primary Microcephaly(ID:disease_node_19276) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)