Disease #00017 (MRXS10 (mental retardation, X-linked syndromic, type 10 (MRXS-10)), OMIM:300220)
| Official abbreviation |
MRXS10 |
| Name |
mental retardation, X-linked syndromic, type 10 (MRXS-10) |
| OMIM ID |
300220 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
4 |
| Associated with 1 gene |
HSD17B10 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2012-07-23 10:48:25 +02:00 (CEST) |
| Date last edited |
2020-05-11 15:16:08 +02:00 (CEST) |
Individuals
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