Phenotype #0000284109

Individual ID 00390572
Associated disease MDDG
Phenotype details congenital muscular dystrophy, mental retardation; 2y7m-walk; no contractures; intellectual disability; no seizures; no eye involvement; CK level 4000 IU/L; MRI brain normal; EMG myogenic; muscle biopsy mild change; EGC normal; UCG normal
Diagnosis/Initial congenital muscular dystrophy, mental retardation
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination 4y7m (4 years, 7 months)
Age/Diagnosis -
Age/Onset 3m
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2021-11-10 16:44:31 +01:00 (CET)
Date last edited N/A

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