Disease #00112 (CAH (Congenital Adrenal Hyperplasia), OMIM:201910)

Official abbreviation CAH
Name Congenital Adrenal Hyperplasia
OMIM ID 201910
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene CYP21A2
Associated tissues -
Disease features -
Remarks -


Individuals

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00000582 P Balraj et al.(2013) - Malaysia Malay - - - CAH salt wasting, simple virilizing CYP21A2 CYP21A2 5 1 Nur Aisyah Athirah
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