Disease #04615 (MCCRP2 (microcephaly and chorioretinopathy, autosomal recessive, type 2 (MCCRP-2)), OMIM:616171)
| Official abbreviation |
MCCRP2 |
| Name |
microcephaly and chorioretinopathy, autosomal recessive, type 2 (MCCRP-2) |
| OMIM ID |
616171 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
PLK4 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:23 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|