Phenotype #0000051928
| Individual ID |
00072222 |
| Associated disease |
? |
| Diagnosis/Initial |
myopathy |
| Diagnosis/Definite |
myopathy, myofibrillar, type 1 (MFM-1) |
| Phenotype details |
Arrhythmia (HP:0011675), atrioventricular block (HP:0001678), right bundle branch block (HP:0011712), atrial flutter (HP:0004749), dilated cardiomyopathy (HP:0001644), severe left ventricle dysfunction (HP:0001711), severe right ventricle dysfunction (HP:0001707), muscular weakness (HP:0001324), pacemaker, Congestive heart failure (HP:0001635) |
| Inheritance |
Familial, autosomal dominant |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Tumor/MSI |
- |
| Diagnosis/Criteria |
- |
| Owner name |
Pieter Klap |
| Database submission license |
No license selected |
| Created by |
Pieter Klap |
| Date created |
2016-06-01 11:30:57 +02:00 (CEST) |
| Date last edited |
2017-09-08 13:02:04 +02:00 (CEST) |
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