Disease #05151 (MCPH9 (microcephaly, type 9, primary, autosomal recessive (MCPH-9)), OMIM:614852)
Official abbreviation |
MCPH9 |
Name |
microcephaly, type 9, primary, autosomal recessive (MCPH-9) |
OMIM ID |
614852 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
CEP152 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2016-04-14 15:46:47 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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