Global Variome shared LOVD

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Phenotype #0000274076 Individual ID 00380224 Associated disease NEDSDV;MRD19 Phenotype details Delayed speech and language development, Global developmental delay, Gait disturbance, Neurological speech impairment, Language impairment, Poor speech, Embryonal neoplasm, Teratoma, Neurodevelopmental delay, Abnormality of movement, Germ cell neoplasia Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination 03y (3 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Birth_Details fetofetal transfusion syndrome, twin sister also with neurodevelopmental delay Protein - Owner name Andreas Laner Database submission license Creative Commons Attribution 4.0 International Created by Andreas Laner Date created 2021-08-12 17:14:41 +02:00 (CEST) Date last edited 2021-08-18 11:48:17 +02:00 (CEST)

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