Disease #03413 (adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete, OMIM:613743)

Official abbreviation -
Name adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete
OMIM ID 613743
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 5
Phenotype entries for this disease 4
Associated with 1 gene CYP11A1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2022-10-03 10:44:38 +02:00 (CEST)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00417410 - - - - - - - - - - - adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete - STAR STAR 1 1 Wenjuan Qiu
00417411 - - - - - (China) - - - - - adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete - STAR STAR 1 1 Wenjuan Qiu
00417412 - - - - - China - - - - - adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete - STAR STAR 1 1 Wenjuan Qiu
00417413 - - - - - - - - - - - adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete - STAR STAR 1 1 Wenjuan Qiu
00417426 - - - - - - - - - - - adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete - STAR STAR 1 1 Wenjuan Qiu
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