Disease #05032 (MRX12;MRX35 (mental retardation, X-linked, type 12/35 (MRX12;MRX35)), OMIM:300957)
| Official abbreviation |
MRX12;MRX35 |
| Name |
mental retardation, X-linked, type 12/35 (MRX12;MRX35) |
| OMIM ID |
300957 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
THOC2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 11:00:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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