Disease #01113 (MCCRP-1 (microcephaly and chorioretinopathy, autosomal recessive, type 1 (MCCRP-1)), OMIM:251270)
| Official abbreviation |
MCCRP-1 |
| Name |
microcephaly and chorioretinopathy, autosomal recessive, type 1 (MCCRP-1) |
| OMIM ID |
251270 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
TUBGCP6 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
