child
stringlengths 4
125
| parent
stringlengths 4
125
| label
int64 0
1
|
|---|---|---|
congenital secretory sodium diarrhea 3
|
idiopathic generalized epilepsy 8
| 0 |
congenital secretory sodium diarrhea 3
|
charcot-marie-tooth disease type 1
| 0 |
congenital secretory sodium diarrhea 3
|
speech disorder
| 0 |
congenital secretory sodium diarrhea 3
|
congenital disorder of glycosylation ig
| 0 |
congenital secretory sodium diarrhea 3
|
gliosarcoma
| 0 |
congenital secretory sodium diarrhea 3
|
stormorken syndrome
| 0 |
congenital secretory sodium diarrhea 3
|
charcot-marie-tooth disease axonal type 2x
| 0 |
congenital secretory sodium diarrhea 3
|
giant cell glioblastoma
| 0 |
hemoglobin c disease
|
hemoglobinopathy
| 1 |
hemoglobin c disease
|
hemoglobin d disease
| 0 |
hemoglobin c disease
|
methemoglobinemia
| 0 |
hemoglobin c disease
|
hemoglobin e disease
| 0 |
hemoglobin c disease
|
schwannoma of twelfth cranial nerve
| 0 |
hemoglobin c disease
|
sotos syndrome 2
| 0 |
hemoglobin c disease
|
myopia
| 0 |
hemoglobin c disease
|
semantic agnosia
| 0 |
hemoglobin c disease
|
coenurosis
| 0 |
hemoglobin c disease
|
sabinas brittle hair syndrome
| 0 |
hemoglobin c disease
|
nominal aphasia
| 0 |
carotid stenosis
|
carotid artery disease
| 1 |
carotid stenosis
|
carotid artery thrombosis
| 0 |
carotid stenosis
|
carotid artery dissection
| 0 |
carotid stenosis
|
mixed hepatoblastoma
| 0 |
carotid stenosis
|
familial isolated trichomegaly
| 0 |
carotid stenosis
|
acute biphenotypic leukemia
| 0 |
carotid stenosis
|
breast fibroadenosis
| 0 |
carotid stenosis
|
primary ciliary dyskinesia 35
| 0 |
carotid stenosis
|
bladder squamous cell carcinoma
| 0 |
carotid stenosis
|
epidural spinal canal neoplasm
| 0 |
carotid stenosis
|
congenital epulis
| 0 |
catecholaminergic polymorphic ventricular tachycardia 4
|
catecholaminergic polymorphic ventricular tachycardia
| 1 |
catecholaminergic polymorphic ventricular tachycardia 4
|
catecholaminergic polymorphic ventricular tachycardia 2
| 0 |
catecholaminergic polymorphic ventricular tachycardia 4
|
catecholaminergic polymorphic ventricular tachycardia 3
| 0 |
catecholaminergic polymorphic ventricular tachycardia 4
|
catecholaminergic polymorphic ventricular tachycardia 1
| 0 |
catecholaminergic polymorphic ventricular tachycardia 4
|
catecholaminergic polymorphic ventricular tachycardia 5
| 0 |
catecholaminergic polymorphic ventricular tachycardia 4
|
autosomal recessive nonsyndromic deafness 25
| 0 |
catecholaminergic polymorphic ventricular tachycardia 4
|
meniere's disease
| 0 |
catecholaminergic polymorphic ventricular tachycardia 4
|
menkes disease
| 0 |
catecholaminergic polymorphic ventricular tachycardia 4
|
saldino-noonan syndrome
| 0 |
catecholaminergic polymorphic ventricular tachycardia 4
|
boutonneuse fever
| 0 |
catecholaminergic polymorphic ventricular tachycardia 4
|
autosomal recessive intellectual developmental disorder 60
| 0 |
myofibrillar myopathy 8
|
myofibrillar myopathy
| 1 |
myofibrillar myopathy 8
|
myofibrillar myopathy 3
| 0 |
myofibrillar myopathy 8
|
myofibrillar myopathy 9
| 0 |
myofibrillar myopathy 8
|
myofibrillar myopathy 5
| 0 |
myofibrillar myopathy 8
|
myofibrillar myopathy 4
| 0 |
myofibrillar myopathy 8
|
myofibrillar myopathy 1
| 0 |
myofibrillar myopathy 8
|
myofibrillar myopathy 6
| 0 |
myofibrillar myopathy 8
|
myofibrillar myopathy 2
| 0 |
myofibrillar myopathy 8
|
fatal infantile hypertonic myofibrillar myopathy
| 0 |
myofibrillar myopathy 8
|
myofibrillar myopathy 10
| 0 |
myofibrillar myopathy 8
|
myofibrillar myopathy 7
| 0 |
familial hemiplegic migraine 3
|
familial hemiplegic migraine
| 1 |
familial hemiplegic migraine 3
|
familial hemiplegic migraine 1
| 0 |
familial hemiplegic migraine 3
|
familial hemiplegic migraine 2
| 0 |
familial hemiplegic migraine 3
|
timothy grass allergy
| 0 |
familial hemiplegic migraine 3
|
distal hereditary motor neuronopathy type 2a
| 0 |
familial hemiplegic migraine 3
|
charcot-marie-tooth disease type 2dd
| 0 |
familial hemiplegic migraine 3
|
desmoplastic infantile ganglioglioma
| 0 |
familial hemiplegic migraine 3
|
angiomyolipoma
| 0 |
familial hemiplegic migraine 3
|
silo filler's disease
| 0 |
familial hemiplegic migraine 3
|
macrotrabecular hepatoblastoma
| 0 |
familial hemiplegic migraine 3
|
eyelid benign neoplasm
| 0 |
constrictive pericarditis
|
pericarditis
| 1 |
constrictive pericarditis
|
chronic rheumatic pericarditis
| 0 |
constrictive pericarditis
|
histoplasmosis pericarditis
| 0 |
constrictive pericarditis
|
dressler's syndrome
| 0 |
constrictive pericarditis
|
heart conduction disease
| 0 |
constrictive pericarditis
|
acute eustachian salpingitis
| 0 |
constrictive pericarditis
|
pseudobulbar palsy
| 0 |
constrictive pericarditis
|
cleidocranial dysplasia
| 0 |
constrictive pericarditis
|
vitamin d-dependent rickets type 1a
| 0 |
constrictive pericarditis
|
salivary gland adenoid cystic carcinoma
| 0 |
constrictive pericarditis
|
platelet-type bleeding disorder 18
| 0 |
pericardium leiomyoma
|
cardiovascular organ benign neoplasm
| 1 |
pericardium leiomyoma
|
benign perivascular tumor
| 0 |
pericardium leiomyoma
|
cerebrovascular benign neoplasm
| 0 |
pericardium leiomyoma
|
heart lipoma
| 0 |
pericardium leiomyoma
|
cardiac granular cell neoplasm
| 0 |
pericardium leiomyoma
|
hemangioma
| 0 |
pericardium leiomyoma
|
venous hemangioma
| 0 |
pericardium leiomyoma
|
benign pericardial teratoma
| 0 |
pericardium leiomyoma
|
benign vascular tumor
| 0 |
pericardium leiomyoma
|
osteopathia striata with cranial sclerosis
| 0 |
pericardium leiomyoma
|
nuclear type mitochondrial complex i deficiency 21
| 0 |
progressive myoclonus epilepsy 4
|
progressive myoclonus epilepsy
| 1 |
progressive myoclonus epilepsy 4
|
progressive myoclonus epilepsy 8
| 0 |
progressive myoclonus epilepsy 4
|
progressive myoclonus epilepsy 9
| 0 |
progressive myoclonus epilepsy 4
|
progressive myoclonus epilepsy 10
| 0 |
progressive myoclonus epilepsy 4
|
unverricht-lundborg syndrome
| 0 |
progressive myoclonus epilepsy 4
|
progressive myoclonus epilepsy 3
| 0 |
progressive myoclonus epilepsy 4
|
progressive myoclonus epilepsy 7
| 0 |
progressive myoclonus epilepsy 4
|
progressive myoclonus epilepsy 6
| 0 |
progressive myoclonus epilepsy 4
|
lafora disease
| 0 |
progressive myoclonus epilepsy 4
|
residual stage corticosteroid-induced glaucoma
| 0 |
progressive myoclonus epilepsy 4
|
autosomal recessive limb-girdle muscular dystrophy type 2h
| 0 |
acute gonococcal cystitis
|
acute cystitis
| 1 |
acute gonococcal cystitis
|
nuclear type mitochondrial complex i deficiency 7
| 0 |
acute gonococcal cystitis
|
alzheimer's disease 5
| 0 |
acute gonococcal cystitis
|
46,xy sex reversal 1
| 0 |
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