Disease #01125 (XLID63 (ntellectual developmental disorder, X-linked, type 63), OMIM:300387)
| Official abbreviation |
XLID63 |
| Name |
ntellectual developmental disorder, X-linked, type 63 |
| OMIM ID |
300387 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked dominant |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ACSL4 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2026-03-16 12:11:28 +01:00 (CET) |
Individuals
|