Global Variome shared LOVD

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

Phenotype #0000309939 Individual ID 00418603 Associated disease CF Inheritance Familial, autosomal recessive Diagnosis/Initial cystic fibrosis, primary immunodeficiency, malabsorption Age/Examination - Diagnosis/Definite - Age/Diagnosis - Age/Onset 00y00m01d Phenotype/Onset - Phenotype details failure to thrive,low weight (weight <3rd percentile, height 10th- 25th percentile); no dysmorphism; normal motor development; normal mental development; no neurological abnormalities; recurrent lower respiratory tract infections; chronic cough, hilar lymphadenopathy; no immunological abnormalities; chronic diarrhea; no cardiovascular abnormalities; recurrent otitis media Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2022-10-01 10:38:21 +02:00 (CEST) Date last edited 2022-10-01 10:49:45 +02:00 (CEST)

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