Phenotype #0000164925

Individual ID 00216473
Associated disease HGPS
Phenotype details combined phenotype of progeria and myopathy
Diagnosis/Initial progeria, syndrome, Hutchinson-Gilford (HGPS);MD
Inheritance Isolated (sporadic)
Diagnosis/Definite HGPS
Age/Examination -
Age/Diagnosis -
Age/Onset 0y
Phenotype/Onset -
Protein -
Owner name Janbernd Kirschner
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen