Global Variome shared LOVD

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

Phenotype #0000207156 Individual ID 00269324 Associated disease - Phenotype details 6m, no history of any serious disorder in family; neonatal period severe hypochromic and microcytic anemia with undetectable serum transferrin Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 00y08m (8 months) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Yessine Amri Database submission license No license selected Created by Yessine Amri Date created 2019-11-19 12:37:08 +01:00 (CET) Date last edited 2019-11-30 12:46:07 +01:00 (CET)

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