Disease #00758 (RSTS2 (Rubinstein-Taybi syndrome, type 2), OMIM:613684)
| Official abbreviation |
RSTS2 |
| Name |
Rubinstein-Taybi syndrome, type 2 |
| OMIM ID |
613684 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
9 |
| Phenotype entries for this disease |
9 |
| Associated with 1 gene |
EP300 |
| Associated tissues |
- |
| Disease features |
intellectual disability (77/80), microcephaly (68/82), long eyelashes (56/69), arched eyebrow (54/77)inferior nasal column (56/73), broad toe (56/79), wide thumb (52/79), high palatal arch (38/66), lateral canthus inferior oblique (43/75), extrauterine growth retardation (51/78) |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2025-07-08 15:51:45 +02:00 (CEST) |
Individuals
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