| C0685838 |
Gonadal dysgenesis XX type deafness |
DO |
Perrault syndrome
|
0050857 |
| C0685838 |
Gonadal dysgenesis XX type deafness |
MONDO |
Perrault syndrome 1
|
0009300 |
| C0685838 |
Gonadal dysgenesis XX type deafness |
MONDO |
Perrault syndrome
|
0017312 |
| C0685838 |
Gonadal dysgenesis XX type deafness |
MSH |
Peroxisomal bifunctional enzyme deficiency
|
C537286 |
| C0685838 |
Gonadal dysgenesis XX type deafness |
MSH |
Gonadal dysgenesis XX type deafness
|
C537286 |
| C0685838 |
Gonadal dysgenesis XX type deafness |
OMIM |
GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS
|
233400 |
| C0685838 |
Gonadal dysgenesis XX type deafness |
OMIM |
PERRAULT SYNDROME 1
|
233400 |
| C0685838 |
Gonadal dysgenesis XX type deafness |
ORDO |
Perrault syndrome
|
2855 |