Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000060417 Individual ID 00080848 Associated disease adrenal hyperplasia Phenotype details Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency (OMIM:201910) Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Daniel Trujillano Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2016-09-07 13:24:08 +02:00 (CEST) Date last edited N/A

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