Disease #02524 (MCPH3 (microcephaly, type 3, autosomal recessive (MCPH-3)), OMIM:604804)

Official abbreviation MCPH3
Name microcephaly, type 3, autosomal recessive (MCPH-3)
OMIM ID 604804
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene CDK5RAP2
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

3 entries on 1 page. Showing entries 1 - 3.
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00080838 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - MCPH3 Microcephaly 3, primary, autosomal recessive (OMIM:604804) CDK5RAP2 CDK5RAP2 1 1 Daniel Trujillano
00359491 - - - M yes Iran - - - - - MCPH3 - CDK5RAP2 CDK5RAP2 1 1 Ehsan Jafarinia
00359492 - - - M yes Iran - - - - - MCPH3 - CDK5RAP2 CDK5RAP2 1 1 Ehsan Jafarinia
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