Disease #05151 (MCPH-9 (microcephaly, type 9, primary, autosomal recessive (MCPH-9)), OMIM:614852)

Official abbreviation MCPH-9
Name microcephaly, type 9, primary, autosomal recessive (MCPH-9)
OMIM ID 614852
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 3
Phenotype entries for this disease 0
Associated with 1 gene CEP152
Associated tissues -
Disease features -
Remarks -


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00206476 - - - F - Canada Acadian (East Canada) - 0 - - MCPH-9 - CEP152 CEP152 2 1 -
00206479 - - - M - Canada Acadian (East Canada) - 0 - - MCPH-9 - CEP152 CEP152 2 1 -
00206483 - - - F - Canada Acadian (East Canada) - 0 - - MCPH-9 - CEP152 CEP152 2 1 -
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