Phenotype #0000174313
| Individual ID |
00233891 |
| Associated disease |
FDH |
| Phenotype details |
has additional features; skin phenotype; skeletal defects (HP:0011842); has oral features; thin protruding ear (HP:0000411); eye anomalies (HP:0000478); |
| Diagnosis/Initial |
Goltz-Gorlin syndrome |
| Inheritance |
Unknown |
| Diagnosis/Definite |
FDH |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Raoul Hennekam |
| Database submission license |
No license selected |
| Created by |
Maria Paola Lombardi |
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