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MIRAGE
primary autosomal recessive microcephaly
Summary
- Synonym
-
- MCPH
- Definition
- A primary microcephaly characterized by microcephaly present at birth, where the brain is small but has normal architecture, and nonprogressive mental retardation that has_material_basis_in an autosomal recessive mutation.
- Super Class
- autosomal recessive disease primary microcephaly
External Links
- Disease Ontology
- DOID:0070296
- Mondo Disease Ontology
- ORDO
- GARD
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 699 | BUB1 | BUB1 mitotic checkpoint serine/threonine kinase | |
| 4001 | LMNB1 | lamin B1 | |
| 9918 | NCAPD2 | non-SMC condensin I complex subunit D2 | |
| 9928 | KIF14 | kinesin family member 14 | |
| 10015 | PDCD6IP | programmed cell death 6 interacting protein | |
| 23310 | NCAPD3 | non-SMC condensin II complex subunit D3 | |
| 55262 | TRAPPC14 | trafficking protein particle complex subunit 14 | |
| 57082 | KNL1 | kinetochore scaffold 1 | |
| 84823 | LMNB2 | lamin B2 | |
| 259266 | ASPM | assembly factor for spindle microtubules |
Related Glycoprotein
