Disease #00530 (CRS3 (craniosynostosis, type 3), OMIM:615314)
| Official abbreviation |
CRS3 |
| Name |
craniosynostosis, type 3 |
| OMIM ID |
615314 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
7 |
| Phenotype entries for this disease |
7 |
| Associated with 1 gene |
TCF12 |
| Associated tissues |
- |
| Disease features |
variable craniosynostosis individually or in combination, coronal and/or agittal skull sutures; congenital dysmorphisms (brachydactyly, ptosis, strabismus); neurodevelopmental impairment may be present |
| Remarks |
- |
| Date created |
2014-09-16 22:49:18 +02:00 (CEST) |
| Date last edited |
2025-11-30 12:02:55 +01:00 (CET) |
Individuals
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