Global Variome shared LOVD

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

Phenotype #0000223949 Individual ID 00296542 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details Abnormal CNS myelination (HP:0011400); Global developmental delay (HP:0001263); Abnormality of nervous system physiology (HP:0012638); Leukodystrophy (HP:0002415); Hyperopic astigmatism (HP:0000484); Abnormality of refraction (HP:0000539) Inheritance Unknown Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Andreas Laner Database submission license Creative Commons Attribution 4.0 International Created by Andreas Laner Date created 2020-04-08 09:52:01 +02:00 (CEST) Date last edited 2020-07-20 09:43:51 +02:00 (CEST)

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