|
Brucella suis caused disease or disorder
|
1190 |
|
|
DNA repair-deficiency disorder
|
21190 |
|
|
MPZ Charcot-Marie-Tooth disease
|
11909 |
|
|
DNA repair deficiency disorders
|
21190 |
|
|
3-beta-hydroxy-delta-5-C27-steroid oxidoreductase deficiency type 1
|
11906 |
|
|
Brucella suis disease or disorder
|
1190 |
|
|
NEFL Charcot-Marie-Tooth disease type 1
|
11902 |
|
|
Charcot-Marie-Tooth disease, demyelinating, type 1F
|
11902 |
|
|
Charcot-Marie-Tooth disease, demyelinating, type 1F; CMT1F
|
http://purl.obolibrary.org/obo/MONDO_0011902 |
|
|
SCN2A benign familial infantile epilepsy
|
11904 |
|
|
porokeratosis 4, disseminated superficial actinic type
|
11900 |
|
