| manager |
|
| language |
- |
| license |
- |
| created at |
2025-11-26 04:53:50 UTC |
| updated at |
2025-11-27 01:00:35 UTC |
|
Mondo ID - Mondo Label
|
30,114 entries
|
There is 0 pattern entry.
|
Klippel-Feil syndrome 1, autosomal dominant
|
0007306 |
|
|
Charcot-Marie-Tooth disease type 1B
|
0007307 |
|
|
Charcot-Marie-Tooth disease type 2A1
|
0007308 |
|
|
Charcot-Marie-Tooth disease type 1A
|
0007309 |
|
|
Charcot-Marie-Tooth disease type 1E
|
0007311 |
|
|
Chiari malformation type I
|
0007316 |
|
|
C1 inhibitor deficiency
|
0007361 |
|
|
Schnyder corneal dystrophy
|
0007374 |
|
|
Meesmann corneal dystrophy
|
0007379 |
|
|
Ramos-Arroyo syndrome
|
0007382 |
|
|
Stern-Lubinsky-Durrie syndrome
|
0007383 |
|
|
TWIST1-related craniosynostosis
|
0007399 |
|
|
Cri-du-chat syndrome
|
0007404 |
|
|
Cyprus facial-neuromusculoskeletal syndrome
|
0007413 |
|
|
Gorham-Stout disease
|
0007414 |
|
