child
stringlengths 4
125
| parent
stringlengths 4
125
| label
int64 0
1
|
|---|---|---|
parietal lobe ependymoma
|
retinopathy of prematurity
| 0 |
parietal lobe ependymoma
|
postinfectious encephalitis
| 0 |
parietal lobe ependymoma
|
congenital nystagmus 6
| 0 |
parietal lobe ependymoma
|
leber congenital amaurosis 9
| 0 |
basilar artery insufficiency
|
transient cerebral ischemia
| 1 |
basilar artery insufficiency
|
vertebrobasilar insufficiency
| 0 |
basilar artery insufficiency
|
vertebral artery insufficiency
| 0 |
basilar artery insufficiency
|
hiatus hernia
| 0 |
basilar artery insufficiency
|
nasal cavity lymphoma
| 0 |
basilar artery insufficiency
|
epicardium cancer
| 0 |
basilar artery insufficiency
|
lenz-majewski hyperostotic dwarfism
| 0 |
basilar artery insufficiency
|
brachial plexus neuritis
| 0 |
basilar artery insufficiency
|
lacrimal gland adenocarcinoma
| 0 |
basilar artery insufficiency
|
kearns-sayre syndrome
| 0 |
basilar artery insufficiency
|
endometrioid ovary carcinoma
| 0 |
hallermann-streiff syndrome
|
syndrome
| 1 |
hallermann-streiff syndrome
|
doors syndrome
| 0 |
hallermann-streiff syndrome
|
ladd syndrome
| 0 |
hallermann-streiff syndrome
|
ollier disease
| 0 |
hallermann-streiff syndrome
|
trichorhinophalangeal syndrome type iii
| 0 |
hallermann-streiff syndrome
|
beckwith-wiedemann syndrome
| 0 |
hallermann-streiff syndrome
|
trichodontoosseous syndrome
| 0 |
hallermann-streiff syndrome
|
kinsship syndrome
| 0 |
hallermann-streiff syndrome
|
proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome
| 0 |
hallermann-streiff syndrome
|
shwachman-diamond syndrome
| 0 |
hallermann-streiff syndrome
|
van der woude syndrome
| 0 |
acute sanguinous otitis media
|
acute transudative otitis media
| 1 |
acute sanguinous otitis media
|
blue drum syndrome
| 0 |
acute sanguinous otitis media
|
acute serous otitis media
| 0 |
acute sanguinous otitis media
|
alzheimer's disease
| 0 |
acute sanguinous otitis media
|
psoriasis 9
| 0 |
acute sanguinous otitis media
|
retinitis pigmentosa 57
| 0 |
acute sanguinous otitis media
|
oblique facial clefting 1
| 0 |
acute sanguinous otitis media
|
holzgreve-wagner-rehder syndrome
| 0 |
acute sanguinous otitis media
|
retinitis pigmentosa 68
| 0 |
acute sanguinous otitis media
|
penicillin allergy
| 0 |
acute sanguinous otitis media
|
dna ligase iv deficiency
| 0 |
reducing body myopathy 1b
|
myopathy
| 1 |
reducing body myopathy 1b
|
myopathy with extrapyramidal signs
| 0 |
reducing body myopathy 1b
|
myositis
| 0 |
reducing body myopathy 1b
|
congenital structural myopathy
| 0 |
reducing body myopathy 1b
|
neurogenic scapuloperoneal syndrome kaeser type
| 0 |
reducing body myopathy 1b
|
mitochondrial myopathy
| 0 |
reducing body myopathy 1b
|
centronuclear myopathy
| 0 |
reducing body myopathy 1b
|
myofascial pain syndrome
| 0 |
reducing body myopathy 1b
|
x-linked myopathy with excessive autophagy
| 0 |
reducing body myopathy 1b
|
gne myopathy
| 0 |
reducing body myopathy 1b
|
muscular dystrophy
| 0 |
malignant adenoma
|
cell type cancer
| 1 |
malignant adenoma
|
germ cell cancer
| 0 |
malignant adenoma
|
carcinoma
| 0 |
malignant adenoma
|
blastoma
| 0 |
malignant adenoma
|
malignant mesothelioma
| 0 |
malignant adenoma
|
mixed cell type cancer
| 0 |
malignant adenoma
|
sarcoma
| 0 |
malignant adenoma
|
high grade glioma
| 0 |
malignant adenoma
|
melanoma
| 0 |
malignant adenoma
|
mesenchymal cell neoplasm
| 0 |
malignant adenoma
|
malignant hemangioma
| 0 |
constant exophthalmos
|
orbital disease
| 1 |
constant exophthalmos
|
endocrine exophthalmos
| 0 |
constant exophthalmos
|
lateral displacement of eye
| 0 |
constant exophthalmos
|
acute orbital inflammation
| 0 |
constant exophthalmos
|
orbital cyst
| 0 |
constant exophthalmos
|
hemangioma of orbit
| 0 |
constant exophthalmos
|
intermittent proptosis
| 0 |
constant exophthalmos
|
pulsating exophthalmos
| 0 |
constant exophthalmos
|
chronic orbital inflammation
| 0 |
constant exophthalmos
|
enophthalmos
| 0 |
constant exophthalmos
|
short-rib thoracic dysplasia 11 with or without polydactyly
| 0 |
spinal cord glioma
|
spinal cancer
| 1 |
spinal cord glioma
|
spinal cord melanoma
| 0 |
spinal cord glioma
|
cauda equina neoplasm
| 0 |
spinal cord glioma
|
conus medullaris neoplasm
| 0 |
spinal cord glioma
|
spinal cord intramedullary teratoma
| 0 |
spinal cord glioma
|
childhood spinal cord tumor
| 0 |
spinal cord glioma
|
spinal cord primitive neuroectodermal neoplasm
| 0 |
spinal cord glioma
|
epidural spinal canal neoplasm
| 0 |
spinal cord glioma
|
spinal cord lymphoma
| 0 |
spinal cord glioma
|
spinal meninges cancer
| 0 |
spinal cord glioma
|
spinal canal and spinal cord meningioma
| 0 |
mediastinum seminoma
|
mediastinal cancer
| 1 |
mediastinum seminoma
|
mediastinal malignant lymphoma
| 0 |
mediastinum seminoma
|
malignant melanocytic peripheral nerve sheath tumor of mediastinum
| 0 |
mediastinum seminoma
|
mediastinum sarcoma
| 0 |
mediastinum seminoma
|
mediastinal mesenchymal tumor
| 0 |
mediastinum seminoma
|
malignant mediastinal neurogenic neoplasm
| 0 |
mediastinum seminoma
|
posterior mediastinum cancer
| 0 |
mediastinum seminoma
|
mediastinum teratoma
| 0 |
mediastinum seminoma
|
autosomal dominant nonsyndromic deafness 48
| 0 |
mediastinum seminoma
|
heart sarcoma
| 0 |
mediastinum seminoma
|
barber-say syndrome
| 0 |
expressive language disorder
|
language disorder
| 1 |
expressive language disorder
|
aphasia
| 0 |
expressive language disorder
|
specific language impairment
| 0 |
expressive language disorder
|
2-aminoadipic 2-oxoadipic aciduria
| 0 |
expressive language disorder
|
myositis ossificans
| 0 |
expressive language disorder
|
bullous skin disease
| 0 |
expressive language disorder
|
plasminogen deficiency type i
| 0 |
expressive language disorder
|
pulmonary interstitial emphysema
| 0 |
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