Disease #00857 (MCPH10 (microcephaly, type 10, primary, autosomal recessive (MCPH-10)), OMIM:615095)

Official abbreviation MCPH10
Name microcephaly, type 10, primary, autosomal recessive (MCPH-10)
OMIM ID 615095
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene ZNF335
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00363847 - - - M yes (Tunisia) - - - - - MCPH10 - ZNF335 ZNF335 1 1 Imen REJEB
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