Phenotype #0000051909
| Individual ID |
00072204 |
| Associated disease |
? |
| Diagnosis/Initial |
myopathy |
| Diagnosis/Definite |
myopathy, myofibrillar, type 1 (MFM-1) |
| Phenotype details |
Palpitations (HP:0001962), unspecified cardiomyopathy (HP:0001638), premature ventricular beat (HP:0004308), Atrial fibrillation (HP:0005110), Right ventricular congestive heart failure (HP:0001635), Limb-girdle muscular dystrophy (HP:0006785), Elevated serum creatine phosphokinase (HP:0003236), Endocardial fibrosis (HP:0006685), |
| Inheritance |
Familial, autosomal dominant |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
Palpitations (HP:0001962), unspecified cardiomyopathy (HP:0001638) |
| Protein |
- |
| Tumor/MSI |
- |
| Diagnosis/Criteria |
- |
| Owner name |
Pieter Klap |
| Database submission license |
No license selected |
| Created by |
Pieter Klap |
| Date created |
2016-05-31 13:34:19 +02:00 (CEST) |
| Date last edited |
2017-09-08 13:02:04 +02:00 (CEST) |
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