Phenotype #0000321804
| Individual ID |
00431195 |
| Associated disease |
? |
| Diagnosis/Initial |
congenital hearing loss, male infertility |
| Diagnosis/Definite |
- |
| Phenotype details |
analysis sperm see paper; assisted reproductive technology; birth-hearing loss, 35y-39y severe/profound hearing loss, no tinnitus, hearing aids, cochlear implant, no vestibular function defect/cochlear malformation, no vertigo |
| Inheritance |
Familial, autosomal recessive |
| Age/Examination |
39y (39 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Tumor/MSI |
- |
| Diagnosis/Criteria |
- |
| Owner name |
Ehsan Jafarinia |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2023-02-01 11:02:25 +01:00 (CET) |
| Date last edited |
N/A |
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