|
Charcot-Marie-Tooth disease, demyelinating, type 1F
|
11902 |
|
|
Charcot-Marie-Tooth disease, demyelinating, type 1F; CMT1F
|
http://purl.obolibrary.org/obo/MONDO_0011902 |
|
|
DNA repair deficiency disorders
|
21190 |
|
|
3-beta-hydroxy-delta-5-C27-steroid oxidoreductase deficiency type 1
|
11906 |
|
|
Brucella suis disease or disorder
|
1190 |
|
|
3-Beta-hydroxy-Delta-5-C27-steroid oxidoreductase deficiency
|
11906 |
|
|
porokeratosis 4, disseminated superficial actinic type
|
11900 |
|
|
DNA repair-deficiency disorder
|
21190 |
|
|
NEFL Charcot-Marie-Tooth disease type 1
|
11902 |
|
|
axonal Charcot-Marie-Tooth disease with pyramidal involvement
|
11901 |
|
