Phenotype #0000125355
| Individual ID |
00103630 |
| Associated disease |
MDC |
| Phenotype details |
elevated serum creatine phosphokinase (HP:0003236), muscular dystrophy (HP:0003560), inability to walk (HP:0002540), feeding difficulties (HP:0011968), scoliosis (HP:0002650), joint contracture (HP:0001371), respiratory insufficiency due to muscle weakness (HP:0002747) |
| Diagnosis/Initial |
dystrophy, muscular, congenital |
| Diagnosis/Definite |
MDC-1A |
| Inheritance |
Familial, autosomal recessive |
| Age/Examination |
04y (4 years) |
| Age/Diagnosis |
- |
| Age/Onset |
00y01m15d |
| Phenotype/Onset |
- |
| Protein |
muscle, IHC for LAMA2, no expression |
| Owner name |
Jorge Oliveira |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Jorge Oliveira |
| Date created |
2017-04-14 19:55:27 +02:00 (CEST) |
| Date last edited |
2019-08-02 19:23:04 +02:00 (CEST) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|