Disease #03931 (CDCBM3 (dysplasia ,cortical, complex, with other brain malformations, type 3 (CDCBM-3)), OMIM:615411)

Official abbreviation CDCBM3
Name dysplasia ,cortical, complex, with other brain malformations, type 3 (CDCBM-3)
OMIM ID 615411
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene KIF2A
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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00435035 - - - M no China Eastern Asian - - - - CDCBM3 - KIF2A KIF2A 1 1 Ke Xu
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