Disease #03277 (CDCBM8 (dysplasia, cortical, complex, with other brain malformations, type 8 (CDCBM8, polymicrogyria)), OMIM:613180)

Official abbreviation CDCBM8
Name dysplasia, cortical, complex, with other brain malformations, type 8 (CDCBM8, polymicrogyria)
OMIM ID 613180
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TUBA8
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-01-10 12:06:43 +01:00 (CET)

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