All terms in MONDO
| Label |
Id |
Description |
|
hemoglobin H disease
|
MONDO_0013512 |
|
|
atrial fibrillation, familial, 9
|
MONDO_0013513 |
|
|
conjugate gaze palsy
|
MONDO_0001527 |
|
|
labia minora cancer
|
MONDO_0001526 |
|
|
capillariasis
|
MONDO_0001532 |
|
|
vaginal leiomyoma
|
MONDO_0001536 |
|
|
vagus nerve disorder
|
MONDO_0001535 |
|
|
ocular hyperemia
|
MONDO_0001534 |
|
|
mink viral enteritis
|
MONDO_0025505 |
|
|
pes anserinus tendinitis or bursitis
|
MONDO_0001533 |
|
|
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3
|
MONDO_0013507 |
|
|
myopia 19, autosomal dominant
|
MONDO_0013508 |
|
|
spermatogenic failure 9
|
MONDO_0013505 |
|
|
schizophrenia 16
|
MONDO_0013506 |
|
|
intellectual disability, autosomal dominant 6
|
MONDO_0013509 |
|
|
dyskeratosis congenita, autosomal dominant 3
|
MONDO_0013522 |
|
|
dyskeratosis congenita, autosomal recessive 3
|
MONDO_0013520 |
|
|
primary ciliary dyskinesia 16
|
MONDO_0013525 |
|
|
progressive myoclonic epilepsy type 6
|
MONDO_0013526 |
|
|
Nestor-Guillermo progeria syndrome
|
MONDO_0013523 |
|
