Phenotype #0000232862

Individual ID 00307037
Associated disease GM1G2
Phenotype details HP:0000708 Behavioral abnormality
HP:0001288 Gait disturbance
HP:0001263 Global developmental delay
HP:0001249 Intellectual disability
HP:0002344 Progressive neurologic deterioration
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis 04y
Age/Onset 03y
Phenotype/Onset -
Protein -
Owner name Sarah Snanoudj
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Sarah Snanoudj
Date created 2020-07-28 17:18:29 +02:00 (CEST)
Date last edited 2020-07-30 12:24:58 +02:00 (CEST)

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