Disease #00709 (MCPH6 (microcephaly, type 6, primary, autosomal recessive (MCPH-6)), OMIM:608393)

Official abbreviation MCPH6
Name microcephaly, type 6, primary, autosomal recessive (MCPH-6)
OMIM ID 608393
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene CENPJ
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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00095095 - - - - no - - - - - - MCPH6 Congenital microcephaly - CENPJ 2 1 Karen Stals
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