National Cancer Institute Thesaurus

Last uploaded: February 21, 2019

Preferred Name	Kallmann Syndrome
ID	http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C75479
code	C75479
DEFINITION	An X-linked or autosomal dominant genetic syndrome characterized by hypogonadotropic hypogonadism and anosmia.
FULL_SYN	Hypogonadotropic Hypogonadism with Anosmia
label	Kallmann Syndrome
Legacy_Concept_Name	Kallmann_Syndrome
Preferred_Name	Kallmann Syndrome
prefixIRI	C75479
prefLabel	Kallmann Syndrome
Semantic_Type	Disease or Syndrome
UMLS_CUI	C0162809
subClassOf	http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C53543 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C28193

Delete	Subject	Author	Type	Created
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Delete	Mapping To	Ontology	Source
	http://purl.obolibrary.org/obo/DOID_3614	Human Disease Ontology 123	LOOM
	http://purl.bioontology.org/ontology/MESH/D017436	Medical Subject Headings	LOOM