Phenotype #0000060797

Individual ID 00081220
Associated disease SRXX2
Phenotype details family, 46,XX testicular disorder of sex development; 1 male (4 children, 2 carrier sons) and 3 adult males (two brothers, paternal uncle) female karyotype (46,XX) and negative for SRY gene.
Diagnosis/Initial -
Inheritance Familial
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2016-09-23 12:58:52 +02:00 (CEST)
Date last edited N/A

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