Disease #01762 (SSPS (Schopf-Schulz-Passarge syndrome (SSPS)), OMIM:224750)

Official abbreviation SSPS
Name Schopf-Schulz-Passarge syndrome (SSPS)
OMIM ID 224750
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene WNT10A
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Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00399462 Pat43 PubMed: Martínez-Romero 2019 - F - Spain - - 0 - - SSPS - WNT10A WNT10A 1 1 Johan den Dunnen
00399467 Pat49 PubMed: Martínez-Romero 2019 - M - Spain - - 0 - - SSPS - WNT10A WNT10A 1 1 Johan den Dunnen
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