Phenotype #0000152878

Individual ID 00204616
Associated disease BVVLS1
Phenotype details Anterior horn neuropathy; Intact cognitive development. Initial presentation: Progressive bulbar palsy
Diagnosis/Initial -
Inheritance -
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Jacopo Celli
Date created 2010-07-22 11:21:10 +02:00 (CEST)
Date last edited 2021-10-24 16:19:28 +02:00 (CEST)

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