Phenotypes for disease #01623 (IAD (ACTH deficiency, isolated (IAD)), OMIM:201400)

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     
0000270476 Congenital ACTH deficiency, secondary adrenal insufficiency - - Familial, autosomal recessive - 06y - - - Andreas Laner 00375265
0000319049 see paper; ... ACTH deficiency IAD Familial, autosomal recessive 00y05m 00y01m - hypoglycemia - Alexandru SAVEANU 00428113
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