All terms in MONDO
| Label |
Id |
Description |
|
premature ovarian failure 14
|
MONDO_0044777 |
|
|
capillary malformation-arteriovenous malformation 1
|
MONDO_0020783 |
|
|
premature ovarian failure 10
|
MONDO_0044776 |
|
|
chronic gingivitis
|
MONDO_0020782 |
|
|
simian immunodeficiency virus infection
|
MONDO_0005163 |
|
|
encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1
|
MONDO_0020781 |
|
|
obsolete influenza infection
|
MONDO_0005162 |
|
|
cone-rod dystrophy and hearing loss 2
|
MONDO_0020780 |
|
|
Stevens-Johnson syndrome/toxic epidermal necrolysis overlap syndrome
|
MONDO_0044739 |
|
|
Gabriele de Vries syndrome
|
MONDO_0044738 |
|
|
neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities
|
MONDO_0032790 |
|
|
obsolete chronic myeloproliferative disorder
|
MONDO_0005171 |
|
|
Usher syndrome, type 4
|
MONDO_0029141 |
|
|
glycosylphosphatidylinositol biosynthesis defect 18
|
MONDO_0029140 |
|
|
autosomal recessive complex spastic paraplegia due to kennedy pathway dysfunction
|
MONDO_0044737 |
|
|
myopathy, congenital, with tremor
|
MONDO_0032797 |
|
|
obsolete pulmonary arterial hypertension associated with chronic hemolytic anemia
|
MONDO_0017156 |
|
|
oculopharyngodistal myopathy 2
|
MONDO_0030134 |
|
|
ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features
|
MONDO_0032798 |
|
|
pulmonary hypertension owing to lung disease and/or hypoxia
|
MONDO_0017157 |
|
