Global Variome shared LOVD

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Phenotype #0000346377 Individual ID 00457927 Associated disease ? Diagnosis/Initial GM3 synthase deficiency Diagnosis/Definite SPDRS Phenotype details see paper; ..., feeding difficulties; profound intellectual disability; not sitting; not walking; nonverbal; absent use of hands; hearing loss; no eye contact; epilepsy; microcephaly (SD-4.4); hypotrophy; dyskinesia, chorea; normal pigmentation skin Inheritance Familial, autosomal recessive Age/Examination 7y6m (7 years, 6 months) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2024-11-21 14:48:01 +01:00 (CET) Date last edited N/A

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