Disease #02495 (MCPH2 (microcephaly, type 2, autosomal recessive, with/without cortical malformations (MCPH-2)), OMIM:604317)

Official abbreviation MCPH2
Name microcephaly, type 2, autosomal recessive, with/without cortical malformations (MCPH-2)
OMIM ID 604317
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene WDR62
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

2 entries on 1 page. Showing entries 1 - 2.
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00081843 FamPatVII2 PubMed: Dincer 2017, Journal: Dincer 2017 relative of FamPatVIII2 M yes Turkey - - - - - MCPH2 Intellectual disability, severe (HP:0010864) Sloping forehead (HP:0000340) Upslanted palpebral fissure (HP:0000582) Blepharophimosis (HP:0000581) Epicanthus (HP:0000286) Prominent nose (HP:0000448) Micrognathia (HP:0000347) PLK4 PLK4 1 1 Bayram Toraman
00331728 WDR62-affected male - - M yes Iran Persian 11y? - - - MCPH2 - WDR62 WDR62 1 1 Ehsan Razmara
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