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Zimmermann-Laband syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0000200

Zimmermann-Laband syndrome (ZLS) is a rare disorder characterized by gingival fibromatosis, coarse facial appearance, and absence or hypoplasia of nails or terminal phalanges of hands and feet. [ Orphanet:3473 ]

Synonyms: Zimmermann-Laband syndrome type 1 gingival fibromatosis-hepatosplenomegaly-other anomalies syndrome Laband syndrome

This is just here as a test because I lose it

Term information

database cross reference
  • ICD9:759.89 (MONDO:relatedTo)
  • OMIMPS:135500 (MONDO:equivalentTo)
  • MESH:C536725 (MONDO:equivalentTo)
  • Orphanet:3473 (OMIM:135500)
  • GARD:385 (MONDO:GARD)
  • UMLS:C0796013 (MONDO:equivalentTo)
  • SCTID:699447001 (MONDO:equivalentTo)
  • MEDGEN:208656 (MONDO:equivalentTo)
Subsets

ordo_disorder, gard_rare, otar, rare, ordo_malformation_syndrome, prototype_pattern, nord_rare, orphanet_rare

exactMatch

http://identifiers.org/medgen/208656

http://www.orpha.net/ORDO/Orphanet_3473

http://identifiers.org/snomedct/699447001

http://identifiers.org/mesh/C536725

http://linkedlifedata.com/resource/umls/id/C0796013

https://omim.org/phenotypicSeries/PS135500

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0015159

http://purl.obolibrary.org/obo/MONDO_0000508

has related synonym

ZLS

Laband-Zimmermann syndrome

Zimmerman Laband syndrome

ZLS1

gingival fibromatosis, abnormal fingers, fingernails, nose and ears, and splenomegaly

fibromatosis gingival, hepatosplenomegaly other anomalies

Zimmermann-Laband syndrome 1

id

MONDO:0000200

Term relations

Subclass of: