Phenotype #0000092140
| Individual ID |
00116692 |
| Associated disease |
IFAP1 |
| Phenotype details |
born with full head of hair. dry and rough skin. hypotrochosis at age 9. mild photophobia. mild myopia; IFAP syndrome; no intellectual disability |
| Diagnosis/Initial |
- |
| Inheritance |
Familial |
| Diagnosis/Definite |
- |
| Age/Examination |
09y (9 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Emmelien Aten |
| Database submission license |
No license selected |
| Created by |
Emmelien Aten |
| Date created |
2011-01-16 20:20:20 +01:00 (CET) |
| Date last edited |
2017-08-08 19:45:17 +02:00 (CEST) |
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