Disease #02209 (MRX101 (mental retardation, X-linked, type 101 (MRX101)), OMIM:300928)
| Official abbreviation |
MRX101 |
| Name |
mental retardation, X-linked, type 101 (MRX101) |
| OMIM ID |
300928 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked recessive |
| Individuals reported having this disease |
5 |
| Phenotype entries for this disease |
5 |
| Associated with 1 gene |
MID2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-05-11 15:17:00 +02:00 (CEST) |
Individuals
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