Autosomal Domit Primary Microcephaly 26
Disease ID: disease_node_19307
Connections displayed (default: 10).
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| Dbxref | MIM:150340 |
|---|---|
| Subclassof | DOID_0050736, DOID_0070297 |
| Data Source | DOID |
| Doid Label | autosomal domit primary microcephaly 26 |
| Doid Description | A primary microcephaly that is characterized by progressive microcephaly beginning at birth and associated with global developmental delay with variably impaired intellectual development and that has_material_basis_in heterozygous mutation in the LMNB1 gene on chromosome 5q23. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_19307 |
| Doid Id | DOID_0051037 |
| Label | Autosomal Domit Primary Microcephaly 26 |
- 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)