Preferred Name |
Denys-Drash syndrome |
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Synonyms |
Denys–Drash syndrome |
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Definitions |
An autosomal dominant disease that is characterized by the association of diffuse mesangial sclerosis (DMS), intersex anatomy with a 46,XY karyotype, and nephroblastoma that derives from an abnormality in the WT1 gene (Wilms' tumor suppressor gene). |
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ID |
http://purl.obolibrary.org/obo/GSSO_006968 |
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definition |
An autosomal dominant disease that is characterized by the association of diffuse mesangial sclerosis (DMS), intersex anatomy with a 46,XY karyotype, and nephroblastoma that derives from an abnormality in the WT1 gene (Wilms' tumor suppressor gene). |
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Disease Ontology ID | ||
has database cross reference |
https://lgbta.fandom.com/wiki/Denys-Drash_Syndrome |
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has exact synonym |
Denys–Drash syndrome Denys Drash syndrome |
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has synonym |
Drash syndrome |
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label |
Denys-Drash syndrome |
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Medical Dictionary for Regulatory Activities ID | ||
MeSH Descriptor ID | ||
NCI Thesaurus ID | ||
prefixIRI |
GSSO:006968 |
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prefLabel |
Denys-Drash syndrome |
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short name |
DDS |
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subClassOf |
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