Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	SCHOPF-SCHULZ-PASSARGE SYNDROME
Synonyms	KERATOSIS PALMOPLANTARIS WITH CYSTIC EYELIDS, HYPODONTIA, AND HYPOTRICHOSIS
ID	http://purl.bioontology.org/ontology/OMIM/224750
altLabel	KERATOSIS PALMOPLANTARIS WITH CYSTIC EYELIDS, HYPODONTIA, AND HYPOTRICHOSIS SSPS ECCRINE TUMORS WITH ECTODERMAL DYSPLASIA
cui	C1857069
Gene Locus	2q35
Gene Symbol	WNT10A STHAG4 OODD SSPS
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU000701 http://purl.bioontology.org/ontology/OMIM/MTHU013255 http://purl.bioontology.org/ontology/OMIM/MTHU013253 http://purl.bioontology.org/ontology/OMIM/MTHU002027 http://purl.bioontology.org/ontology/OMIM/MTHU007784 http://purl.bioontology.org/ontology/OMIM/MTHU037397 http://purl.bioontology.org/ontology/OMIM/MTHU003747 http://purl.bioontology.org/ontology/OMIM/MTHU000129 http://purl.bioontology.org/ontology/OMIM/MTHU013254 http://purl.bioontology.org/ontology/OMIM/MTHU013252 http://purl.bioontology.org/ontology/OMIM/MTHU036696 http://purl.bioontology.org/ontology/OMIM/MTHU000128 http://purl.bioontology.org/ontology/OMIM/MTHU013257 http://purl.bioontology.org/ontology/OMIM/MTHU002570
MIMTYPEMEANING	Phenotype description, molecular basis known.
Moved from	600077
notation	224750
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	SCHOPF-SCHULZ-PASSARGE SYNDROME
tui	T047

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/DOID_0111647	Human Disease Ontology 123	LOOM
http://purl.bioontology.org/ontology/MESH/C565607	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/MESH/C565607	Medical Subject Headings	LOOM