Disease #05740 (XLID103 (intellectual developmental disorder, X-linked, type 103), OMIM:300982)
| Official abbreviation |
XLID103 |
| Name |
intellectual developmental disorder, X-linked, type 103 |
| OMIM ID |
300982 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
KLHL15 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-05-11 15:12:58 +02:00 (CEST) |
| Date last edited |
2023-10-23 16:36:10 +02:00 (CEST) |
Individuals
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