Phenotype #0000130108
| Individual ID |
00165222 |
| Associated disease |
STL |
| Phenotype details |
HP:0000541 Retinal detachment HP:0000545 Myopia HP:0000407 Sensorineural hearing impairment HP:0000278 Retrognathia |
| Diagnosis/Initial |
Type 2 Stickler syndrome |
| Inheritance |
Familial, autosomal dominant |
| Diagnosis/Definite |
Stickler syndrome |
| Age/Examination |
41y (41 years) |
| Age/Diagnosis |
41y |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Thomas Nixon |
| Database submission license |
No license selected |
| Created by |
Thomas Nixon |
| Date created |
2018-07-02 17:05:50 +02:00 (CEST) |
| Date last edited |
2018-07-03 16:08:12 +02:00 (CEST) |
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