Phenotypes for disease #01632 (GCCD1 (glucocorticoid deficiency, due to ACTH unresponsiveness (GCCD1, ACTH resistance)), OMIM:202200)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000239782 hyperpigmentation - Familial Glucocorticoid Deficiency Familial, autosomal recessive 03y 03y - - - Wenjuan Qiu 00316036
0000278438 very high levels of ACTH Neonatal cholestasis - Familial, autosomal recessive - - - - - Annalaura Torella 00384654
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