Global Variome shared LOVD

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

Phenotype #0000017789 Individual ID 00020026 Associated disease FANCP Phenotype details prenatal dystrophy, short stature, hypoplasia right thumb, microcephaly, hyperpigmentation, cafÈ-au-lait, vitiligo, hypothyreoidism Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Beatrice Schuster Database submission license No license selected Created by Arleen D. Auerbach Date created 2012-10-15 01:30:14 +02:00 (CEST) Date last edited 2014-10-11 14:14:00 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.