Disease #06626 (MCPH18 (microcephaly 18, primary, autosomal dominant), OMIM:617520)
| Official abbreviation |
MCPH18 |
| Name |
microcephaly 18, primary, autosomal dominant |
| OMIM ID |
617520 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
WDFY3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
2024-12-03 09:55:53 +01:00 (CET) |
Individuals
|