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
Disease Ontology
DOID:0070296
Mondo Disease Ontology
ORDO
OMIM
GARD
Related Genes
Displaying entries 1 - 10 of 11 in total
Gene ID Gene Symbol Description Source
1781 DYNC1I2 dynein cytoplasmic 1 intermediate chain 2
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
Displaying all 6 entries
Gene ID Gene Symbol Description Source
12235 Bub1 BUB1, mitotic checkpoint serine/threonine kinase
16906 Lmnb1 lamin B1
16907 Lmnb2 lamin B2
18571 Pdcd6ip programmed cell death 6 interacting protein
78658 Ncapd3 non-SMC condensin II complex, subunit D3
215387 Ncaph non-SMC condensin I complex, subunit H
Displaying 1 entry
Gene ID Gene Symbol Description Source
116685 Lmnb1 lamin B1
Displaying 1 entry
Gene ID Gene Symbol Description Source
40859 Sas-4 Spindle assembly abnormal 4

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Last updated: December 9, 2024