Phenotype #0000015234
| Individual ID |
00016720 |
| Associated disease |
DA5 |
| Phenotype details |
contractures hand/feet; III7 mild ptosis; ophthalmoplegia (except II6); I2/II2/II5 pulmonary disease |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal dominant |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Marianne Vos (LOVD-team) |
| Database submission license |
No license selected |
| Created by |
Marianne Vos (LOVD-team) |
| Date created |
2014-05-27 13:26:55 +02:00 (CEST) |
| Date last edited |
2015-09-11 19:47:11 +02:00 (CEST) |
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