Phenotype #0000319049

Individual ID 00428113
Associated disease IAD
Phenotype details see paper; ...
Diagnosis/Initial ACTH deficiency
Inheritance Familial, autosomal recessive
Diagnosis/Definite IAD
Age/Examination 00y05m (5 months)
Age/Diagnosis 00y01m
Age/Onset -
Phenotype/Onset hypoglycemia
Protein -
Owner name Alexandru SAVEANU
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Alexandru SAVEANU
Date created 2022-12-22 11:25:17 +01:00 (CET)
Date last edited 2025-01-23 19:56:19 +01:00 (CET)

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