Individual ID |
00234923 |
Associated disease |
GSD2 |
Phenotype details |
age onset 2y/38y; age analysis 2y/63y; no respiratory problems (-HP:0002795)/respiratory problems (HP:0002795) ; no mobility problem (-HP:0100022)/mobility problem (HP:0100022) |
Diagnosis/Initial |
glycogen storage disease |
Inheritance |
Familial, autosomal recessive |
Diagnosis/Definite |
GSD-2: Childhood (1)/ Adult (1) |
Age/Examination |
- |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Pim Pijnappel |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2019-05-10 13:10:57 +02:00 (CEST) |
Date last edited |
N/A |