Disease #02203 (XLID98;MRX98 (intellectual developmental disorder, X-linked, type 98 (MRX98)), OMIM:300912)
| Official abbreviation |
XLID98;MRX98 |
| Name |
intellectual developmental disorder, X-linked, type 98 (MRX98) |
| OMIM ID |
300912 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked dominant |
| Individuals reported having this disease |
5 |
| Phenotype entries for this disease |
4 |
| Associated with 1 gene |
KIAA2022 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2024-03-12 15:28:19 +01:00 (CET) |
Individuals
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