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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