Disease #00866 (PPS (popliteal pterygium syndrome), OMIM:119500)
| Official abbreviation |
PPS |
| Name |
popliteal pterygium syndrome |
| OMIM ID |
119500 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
IRF6 |
| Associated tissues |
- |
| Disease features |
orofacial clefting; pterygia; ankyloblepharon; oral synechia; syndactyly; genital hypoplasia; no sparse hair; lip pits; nails; hypodontia |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2025-02-06 15:17:19 +01:00 (CET) |
Individuals
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