Phenotype #0000175370

Individual ID 00235106
Associated disease GSD2
Phenotype details age onset 8m-18m; no cardiomyopathy (-HP:0001638); respiratory problems (HP:0002795); mobility problem (HP:0100022)
Diagnosis/Initial glycogen storage disease
Inheritance Familial, autosomal recessive
Diagnosis/Definite GSD-2: childhood onset
Age/Examination 1y11m (1 year, 11 months)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Pim Pijnappel
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-05-10 13:10:57 +02:00 (CEST)
Date last edited N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.