Global Variome shared LOVD

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

Phenotype #0000174776 Individual ID 00234358 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details Global developmental delay (HP:0001263); Intellectual disability, mild (HP:0001256); Muscular hypotonia (HP:0001252); Obesity (HP:0001513); High forehead (HP:0000348); Numerous nevi (HP:0001054); Seizures (HP:0001250); Abnormal social behavior (HP:0012433); Depressivity (HP:0000716); Scoliosis (HP:0002650) Inheritance Unknown Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name IMGAG Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by IMGAG Date created 2019-05-10 11:40:56 +02:00 (CEST) Date last edited 2020-04-01 13:57:49 +02:00 (CEST)

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