All terms in MONDO
| Label |
Id |
Description |
|
intellectual developmental disorder 59
|
MONDO_0032795 |
|
|
obsolete pulmonary hypertension with unclear multifactorial mechanism
|
MONDO_0017158 |
|
|
obsolete syndrome with pulmonary hypertension as a major feature
|
MONDO_0017159 |
|
|
hyper-IgE recurrent infection syndrome 4, autosomal recessive
|
MONDO_0032796 |
|
|
O'Donnell-Luria-Rodan syndrome
|
MONDO_0032793 |
|
|
obsolete pulmonary arterial hypertension associated with congenital heart disease
|
MONDO_0017152 |
|
|
retinitis pigmentosa 96
|
MONDO_0859367 |
|
|
leber congenital amaurosis 19
|
MONDO_0032794 |
|
|
obsolete pulmonary arterial hypertension associated with HIV infection
|
MONDO_0017153 |
|
|
short QT syndrome 7
|
MONDO_0859368 |
|
|
Coffin-Siris syndrome 10
|
MONDO_0032791 |
|
|
obsolete pulmonary arterial hypertension associated with portal hypertension
|
MONDO_0017154 |
|
|
joint contractures, osteochondromas, and B-cell lymphoma
|
MONDO_0859369 |
|
|
obsolete pulmonary arterial hypertension associated with schistosomiasis
|
MONDO_0017155 |
|
|
neuropathy, hereditary motor and sensory, type VIc, with optic atrophy
|
MONDO_0032792 |
|
|
spastic paraplegia 79A, autosomal dominant, with ataxia
|
MONDO_0859363 |
|
|
spermatogenic failure 80
|
MONDO_0859364 |
|
|
obsolete pulmonary arterial hypertension associated with another disease
|
MONDO_0017150 |
|
|
neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures
|
MONDO_0859365 |
|
|
obsolete pulmonary arterial hypertension associated with connective tissue disease
|
MONDO_0017151 |
|