Preferred Name | Kallmann Syndrome | |
Synonyms |
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ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Kallmann_Syndrome |
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DEFINITION |
An X-linked or autosomal dominant genetic syndrome characterized by hypogonadotropic hypogonadism and anosmia. |
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label |
Kallmann Syndrome |
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prefixIRI |
Thesaurus:Kallmann_Syndrome |
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prefLabel |
Kallmann Syndrome |
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subClassOf |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Rare_Non-Neoplastic_Disorder |
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