Global Variome shared LOVD

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

Phenotype #0000223818 Individual ID 00296404 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details Microcephaly (HP:0000252); Intellectual disability (HP:0001249); Seizures (HP:0001250); Global developmental delay (HP:0001263); Cerebellar atrophy (HP:0001272); Hypoplasia of the corpus callosum (HP:0002079); Abnormal morphology of the hippocampus (HP:0025100) 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 2020-04-06 09:48:29 +02:00 (CEST) Date last edited 2020-04-07 04:10:50 +02:00 (CEST)

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