Disease #00010 (MCLMR (microcephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR)), OMIM:152950)
| Official abbreviation |
MCLMR |
| Name |
microcephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR) |
| OMIM ID |
152950 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
KIF11 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2012-06-29 16:51:23 +02:00 (CEST) |
| Date last edited |
N/A |
|
