All terms in MONDO
| Label |
Id |
Description |
|
DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion
|
MONDO_0017056 |
|
|
Galloway-Mowat syndrome 8
|
MONDO_0032693 |
|
|
obsolete chromosome 17q11.2 duplication syndrome, 1.4-mb
|
MONDO_0030032 |
|
|
intraocular medulloepithelioma
|
MONDO_0017050 |
|
|
classic maple syrup urine disease
|
MONDO_0017051 |
|
|
intermediate maple syrup urine disease
|
MONDO_0017052 |
|
|
obsolete short rib-polydactyly syndrome type 5
|
MONDO_0044680 |
|
|
neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline
|
MONDO_0030028 |
|
|
tremor, hereditary essential, 6
|
MONDO_0030027 |
|
|
retinitis pigmentosa 85
|
MONDO_0032689 |
|
|
skeletal dysplasia, mild, with joint laxity and advanced bone age
|
MONDO_0030029 |
|
|
chronic relapsing inflammatory optic neuropathy
|
MONDO_0044687 |
|
|
autoimmune/inflammatory optic neuropathy
|
MONDO_0044685 |
|
|
phyllodes tumor
|
MONDO_0005078 |
|
|
recurrent idiopathic neuroretinitis
|
MONDO_0044689 |
|
|
isolated optic neuritis
|
MONDO_0044688 |
|
|
obsolete limbic encephalitis with neurexin-3 antibodies
|
MONDO_0044683 |
|
|
MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome
|
MONDO_0044682 |
|
|
pertussis
|
MONDO_0005077 |
|
|
bordetellosis
|
MONDO_0037872 |
|
