All terms in MONDO
| Label |
Id |
Description |
|
sarcomatoid renal cell carcinoma
|
MONDO_0003012 |
|
|
obsolete pseudohypoaldosteronism
|
MONDO_0003013 |
|
|
Blastocystis infectious disease
|
MONDO_0005671 |
|
|
blackwater fever
|
MONDO_0005670 |
|
|
spastic paraplegia, intellectual disability, nystagmus, and obesity;
|
MONDO_0015007 |
|
|
epidermolysis bullosa simplex 6, generalized, with scarring and hair loss
|
MONDO_0015006 |
|
|
epilepsy, early-onset, vitamin B6-dependent
|
MONDO_0015005 |
|
|
dystonia 28, childhood-onset
|
MONDO_0015004 |
|
|
lymphatic malformation 7
|
MONDO_0015009 |
|
|
intellectual disability-short stature-hypertelorism syndrome
|
MONDO_0017668 |
|
|
obsolete disease with diffuse palmoplantar keratoderma as a major feature
|
MONDO_0017669 |
|
|
amelogenesis imperfecta, type 1J
|
MONDO_0015008 |
|
|
obsolete miscellaneous movement disorder due to genetic neurodegenerative disease
|
MONDO_0017662 |
|
|
obsolete inherited tremor disorder
|
MONDO_0017663 |
|
|
obsolete rare genetic myoclonus
|
MONDO_0017664 |
|
|
obsolete rare genetic disease with myoclonus as a major feature
|
MONDO_0017665 |
|
|
dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities
|
MONDO_0015003 |
|
|
developmental and epileptic encephalopathy, 49
|
MONDO_0015002 |
|
|
atrial fibrillation, familial, 18
|
MONDO_0015001 |
|
|
obsolete rare genetic parkinsonian disorder
|
MONDO_0017660 |
|
