child
stringlengths 4
125
| parent
stringlengths 4
125
| label
int64 0
1
|
|---|---|---|
alexander disease
|
adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
| 0 |
alexander disease
|
cadasil
| 0 |
alexander disease
|
leukoencephalopathy with vanishing white matter
| 0 |
alexander disease
|
canavan disease
| 0 |
alexander disease
|
rnaset2-deficient cystic leukoencephalopathy
| 0 |
alexander disease
|
cervical benign neoplasm
| 0 |
hyperopia
|
refractive error
| 1 |
hyperopia
|
myopia
| 0 |
hyperopia
|
anisometropia
| 0 |
hyperopia
|
transient refractive change
| 0 |
hyperopia
|
astigmatism
| 0 |
hyperopia
|
aniseikonia
| 0 |
hyperopia
|
combined oxidative phosphorylation deficiency 30
| 0 |
hyperopia
|
trigeminal nerve disease
| 0 |
hyperopia
|
ear cancer
| 0 |
hyperopia
|
subvalvular aortic stenosis
| 0 |
hyperopia
|
cobalt allergic asthma
| 0 |
muscular dystrophy-dystroglycanopathy type b3
|
muscular dystrophy-dystroglycanopathy type b
| 1 |
muscular dystrophy-dystroglycanopathy type b3
|
muscular dystrophy-dystroglycanopathy type b5
| 0 |
muscular dystrophy-dystroglycanopathy type b3
|
muscular dystrophy-dystroglycanopathy type b15
| 0 |
muscular dystrophy-dystroglycanopathy type b3
|
muscular dystrophy-dystroglycanopathy type b4
| 0 |
muscular dystrophy-dystroglycanopathy type b3
|
muscular dystrophy-dystroglycanopathy type b2
| 0 |
muscular dystrophy-dystroglycanopathy type b3
|
muscular dystrophy-dystroglycanopathy type b1
| 0 |
muscular dystrophy-dystroglycanopathy type b3
|
muscular dystrophy-dystroglycanopathy type b6
| 0 |
muscular dystrophy-dystroglycanopathy type b3
|
muscular dystrophy-dystroglycanopathy type b14
| 0 |
muscular dystrophy-dystroglycanopathy type b3
|
open-angle glaucoma
| 0 |
muscular dystrophy-dystroglycanopathy type b3
|
pyridoxine deficiency anemia
| 0 |
muscular dystrophy-dystroglycanopathy type b3
|
xeroderma of eyelid
| 0 |
generalized epilepsy with febrile seizures plus 9
|
generalized epilepsy with febrile seizures plus
| 1 |
generalized epilepsy with febrile seizures plus 9
|
generalized epilepsy with febrile seizures plus 10
| 0 |
generalized epilepsy with febrile seizures plus 9
|
generalized epilepsy with febrile seizures plus 2
| 0 |
generalized epilepsy with febrile seizures plus 9
|
generalized epilepsy with febrile seizures plus 7
| 0 |
generalized epilepsy with febrile seizures plus 9
|
generalized epilepsy with febrile seizures plus 8
| 0 |
generalized epilepsy with febrile seizures plus 9
|
generalized epilepsy with febrile seizures plus 6
| 0 |
generalized epilepsy with febrile seizures plus 9
|
generalized epilepsy with febrile seizures plus 1
| 0 |
generalized epilepsy with febrile seizures plus 9
|
generalized epilepsy with febrile seizures plus 4
| 0 |
generalized epilepsy with febrile seizures plus 9
|
familial visceral amyloidosis
| 0 |
generalized epilepsy with febrile seizures plus 9
|
alpha-2-plasmin inhibitor deficiency
| 0 |
generalized epilepsy with febrile seizures plus 9
|
vacterl association
| 0 |
autosomal recessive osteopetrosis 3
|
osteopetrosis
| 1 |
autosomal recessive osteopetrosis 3
|
autosomal recessive osteopetrosis 2
| 0 |
autosomal recessive osteopetrosis 3
|
autosomal recessive osteopetrosis 5
| 0 |
autosomal recessive osteopetrosis 3
|
autosomal recessive osteopetrosis 6
| 0 |
autosomal recessive osteopetrosis 3
|
autosomal recessive osteopetrosis 4
| 0 |
autosomal recessive osteopetrosis 3
|
autosomal dominant osteopetrosis 2
| 0 |
autosomal recessive osteopetrosis 3
|
autosomal recessive osteopetrosis 1
| 0 |
autosomal recessive osteopetrosis 3
|
autosomal recessive osteopetrosis 7
| 0 |
autosomal recessive osteopetrosis 3
|
autosomal dominant osteopetrosis 1
| 0 |
autosomal recessive osteopetrosis 3
|
autosomal recessive osteopetrosis 8
| 0 |
autosomal recessive osteopetrosis 3
|
ketoprofen photoallergic dermatitis
| 0 |
hypomyelinating leukodystrophy 13
|
hypomyelinating leukodystrophy
| 1 |
hypomyelinating leukodystrophy 13
|
hypomyelinating leukodystrophy 14
| 0 |
hypomyelinating leukodystrophy 13
|
hypomyelinating leukodystrophy 5
| 0 |
hypomyelinating leukodystrophy 13
|
hypomyelinating leukodystrophy 20
| 0 |
hypomyelinating leukodystrophy 13
|
hypomyelinating leukodystrophy 2
| 0 |
hypomyelinating leukodystrophy 13
|
hypomyelinating leukodystrophy 10
| 0 |
hypomyelinating leukodystrophy 13
|
hypomyelinating leukodystrophy 12
| 0 |
hypomyelinating leukodystrophy 13
|
hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism
| 0 |
hypomyelinating leukodystrophy 13
|
hypomyelinating leukodystrophy 11
| 0 |
hypomyelinating leukodystrophy 13
|
hypomyelinating leukodystrophy 4
| 0 |
hypomyelinating leukodystrophy 13
|
hypomyelinating leukodystrophy 6
| 0 |
fanconi anemia complementation group i
|
fanconi anemia
| 1 |
fanconi anemia complementation group i
|
fanconi anemia complementation group d2
| 0 |
fanconi anemia complementation group i
|
fanconi anemia complementation group l
| 0 |
fanconi anemia complementation group i
|
fanconi anemia complementation group p
| 0 |
fanconi anemia complementation group i
|
fanconi anemia complementation group c
| 0 |
fanconi anemia complementation group i
|
fanconi anemia complementation group a
| 0 |
fanconi anemia complementation group i
|
fanconi anemia complementation group o
| 0 |
fanconi anemia complementation group i
|
fanconi anemia complementation group b
| 0 |
fanconi anemia complementation group i
|
fanconi anemia complementation group g
| 0 |
fanconi anemia complementation group i
|
fanconi anemia complementation group f
| 0 |
fanconi anemia complementation group i
|
fanconi anemia complementation group q
| 0 |
ornithine carbamoyltransferase deficiency
|
urea cycle disorder
| 1 |
ornithine carbamoyltransferase deficiency
|
n-acetylglutamate synthase deficiency
| 0 |
ornithine carbamoyltransferase deficiency
|
carbamoyl phosphate synthetase i deficiency disease
| 0 |
ornithine carbamoyltransferase deficiency
|
hyperargininemia
| 0 |
ornithine carbamoyltransferase deficiency
|
citrullinemia
| 0 |
ornithine carbamoyltransferase deficiency
|
multiple epiphyseal dysplasia 1
| 0 |
ornithine carbamoyltransferase deficiency
|
hantavirus pulmonary syndrome
| 0 |
ornithine carbamoyltransferase deficiency
|
filarial elephantiasis
| 0 |
ornithine carbamoyltransferase deficiency
|
autosomal dominant emery-dreifuss muscular dystrophy 2
| 0 |
ornithine carbamoyltransferase deficiency
|
bardet-biedl syndrome 8
| 0 |
ornithine carbamoyltransferase deficiency
|
acute myeloid leukemia with mll rearrangement
| 0 |
familial hemiplegic migraine 1
|
familial hemiplegic migraine
| 1 |
familial hemiplegic migraine 1
|
familial hemiplegic migraine 3
| 0 |
familial hemiplegic migraine 1
|
familial hemiplegic migraine 2
| 0 |
familial hemiplegic migraine 1
|
macular keratitis
| 0 |
familial hemiplegic migraine 1
|
tooth and nail syndrome
| 0 |
familial hemiplegic migraine 1
|
hemochromatosis type 2
| 0 |
familial hemiplegic migraine 1
|
multiple endocrine neoplasia type 2a
| 0 |
familial hemiplegic migraine 1
|
cockayne syndrome b
| 0 |
familial hemiplegic migraine 1
|
gonadoblastoma
| 0 |
familial hemiplegic migraine 1
|
hypomyelinating leukodystrophy 10
| 0 |
familial hemiplegic migraine 1
|
diffuse secondary choroid atrophy
| 0 |
infantile cerebellar-retinal degeneration
|
neurodegenerative disease
| 1 |
infantile cerebellar-retinal degeneration
|
huntington's disease-like 2
| 0 |
infantile cerebellar-retinal degeneration
|
olivopontocerebellar atrophy
| 0 |
infantile cerebellar-retinal degeneration
|
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
| 0 |
infantile cerebellar-retinal degeneration
|
neuroacanthocytosis
| 0 |
infantile cerebellar-retinal degeneration
|
huntington's disease
| 0 |
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