Disease #02272 (SRXX1 (46,XX sex reversal, type 1 (SRXX-1)), OMIM:400045)

Official abbreviation SRXX1
Name 46,XX sex reversal, type 1 (SRXX-1)
OMIM ID 400045
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene SRY
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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