Disease #05531 (CLABARS;MRD49 (Clark-Baraitser syndrome (CLABARS, MRD-49)), OMIM:617752)
| Official abbreviation |
CLABARS;MRD49 |
| Name |
Clark-Baraitser syndrome (CLABARS, MRD-49) |
| OMIM ID |
617752 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
TRIP12 |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
| Date created |
2018-12-18 09:17:05 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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