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

3 entries on 1 page. Showing entries 1 - 3.
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00462242 PPS1 PubMed: Leslie 2015 3-generation family, 1 affected, unaffected heterozygous carrier parents/relatives M yes - - - - - - PPS see paper; ..., orofacial clefting; pterygia; ankyloblepharon; oral synechia; syndactyly; genital hypoplasia; no sparse hair; lip pits IRF6 IRF6 1 1 Johan den Dunnen
00462243 PPS2 PubMed: Leslie 2015 3-generation family, 1 affected, unaffected heterozygous carrier parents/relatives F no - - - - - - PPS see paper; ..., orofacial clefting; pterygia; ankyloblepharon; oral synechia; no syndactyly; genital hypoplasia; sparse hair; lip pits RIPK4 RIPK4 2 1 Johan den Dunnen
00462244 PPS3 PubMed: Leslie 2015 2-generation family, 1 affected, unaffected heterozygous carrier parents M yes - - - - - - PPS see paper; ..., orofacial clefting; pterygia; no ankyloblepharon; oral synechia; syndactyly; genital hypoplasia; sparse hair; no lip pits; dysplastic nails; hypodontia; dramatic malformation of the toes RIPK4 RIPK4 1 1 Johan den Dunnen
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