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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