child
stringlengths 4
125
| parent
stringlengths 4
125
| label
int64 0
1
|
|---|---|---|
intestinal tuberculosis
|
gastrointestinal tuberculosis
| 1 |
intestinal tuberculosis
|
tuberculous peritonitis
| 0 |
intestinal tuberculosis
|
esophageal tuberculosis
| 0 |
intestinal tuberculosis
|
oral tuberculosis
| 0 |
intestinal tuberculosis
|
hepatic tuberculosis
| 0 |
intestinal tuberculosis
|
seminal vesicle chronic gonorrhea
| 0 |
intestinal tuberculosis
|
hypervitaminosis a
| 0 |
intestinal tuberculosis
|
dilated cardiomyopathy 2f
| 0 |
intestinal tuberculosis
|
angiokeratoma
| 0 |
intestinal tuberculosis
|
autosomal recessive congenital bilateral absence of vas deferens
| 0 |
intestinal tuberculosis
|
jejunal adenocarcinoma
| 0 |
familial episodic pain syndrome 1
|
familial episodic pain syndrome
| 1 |
familial episodic pain syndrome 1
|
familial episodic pain syndrome 2
| 0 |
familial episodic pain syndrome 1
|
familial episodic pain syndrome 3
| 0 |
familial episodic pain syndrome 1
|
autosomal recessive limb-girdle muscular dystrophy type 2a
| 0 |
familial episodic pain syndrome 1
|
pancreatic delta cell neoplasm
| 0 |
familial episodic pain syndrome 1
|
langerhans cell sarcoma
| 0 |
familial episodic pain syndrome 1
|
primary ciliary dyskinesia 40
| 0 |
familial episodic pain syndrome 1
|
myeloid sarcoma
| 0 |
familial episodic pain syndrome 1
|
nuclear type mitochondrial complex i deficiency 24
| 0 |
familial episodic pain syndrome 1
|
severe acute respiratory syndrome
| 0 |
familial episodic pain syndrome 1
|
brachial plexus neuropathy
| 0 |
dentine erosion
|
tooth erosion
| 1 |
dentine erosion
|
enamel erosion
| 0 |
dentine erosion
|
pulp erosion
| 0 |
dentine erosion
|
gait apraxia
| 0 |
dentine erosion
|
oculocutaneous albinism type ia
| 0 |
dentine erosion
|
keratosis follicularis spinulosa decalvans
| 0 |
dentine erosion
|
hermansky-pudlak syndrome 2
| 0 |
dentine erosion
|
male reproductive system disease
| 0 |
dentine erosion
|
torsion dystonia 17
| 0 |
dentine erosion
|
arthrogryposis, renal dysfunction, and cholestasis 2
| 0 |
dentine erosion
|
primary polycythemia
| 0 |
anauxetic dysplasia
|
spondyloepimetaphyseal dysplasia
| 1 |
anauxetic dysplasia
|
spondyloepimetaphyseal dysplasia, genevieve-type
| 0 |
anauxetic dysplasia
|
dyggve-melchior-clausen disease
| 0 |
anauxetic dysplasia
|
schimke immuno-osseous dysplasia
| 0 |
anauxetic dysplasia
|
spondyloepimetaphyseal dysplasia, pakistani type
| 0 |
anauxetic dysplasia
|
spondylometaepiphyseal dysplasia, short limb-hand type
| 0 |
anauxetic dysplasia
|
metatropic dysplasia
| 0 |
anauxetic dysplasia
|
spondyloepimetaphyseal dysplasia with joint laxity
| 0 |
anauxetic dysplasia
|
spondyloepimetaphyseal dysplasia, sponastrime type
| 0 |
anauxetic dysplasia
|
x-linked spondyloepimetaphyseal dysplasia
| 0 |
anauxetic dysplasia
|
spondyloepimetaphyseal dysplasia, missouri type
| 0 |
hodgkin's lymphoma, lymphocytic depletion
|
hodgkin's lymphoma
| 1 |
hodgkin's lymphoma, lymphocytic depletion
|
hodgkin's lymphoma, nodular sclerosis
| 0 |
hodgkin's lymphoma, lymphocytic depletion
|
hodgkin's lymphoma, mixed cellularity
| 0 |
hodgkin's lymphoma, lymphocytic depletion
|
hodgkin's lymphoma, lymphocytic-histiocytic predominance
| 0 |
hodgkin's lymphoma, lymphocytic depletion
|
hodgkin's granuloma
| 0 |
hodgkin's lymphoma, lymphocytic depletion
|
hodgkin's paragranuloma
| 0 |
hodgkin's lymphoma, lymphocytic depletion
|
axenfeld-rieger syndrome type 3
| 0 |
hodgkin's lymphoma, lymphocytic depletion
|
hypertrophic cardiomyopathy 15
| 0 |
hodgkin's lymphoma, lymphocytic depletion
|
kindler syndrome
| 0 |
hodgkin's lymphoma, lymphocytic depletion
|
lacrimal gland mucoepidermoid carcinoma
| 0 |
hodgkin's lymphoma, lymphocytic depletion
|
autosomal recessive limb-girdle muscular dystrophy type 2k
| 0 |
very long chain acyl-coa dehydrogenase deficiency
|
lipid metabolism disorder
| 1 |
very long chain acyl-coa dehydrogenase deficiency
|
familial hyperlipidemia
| 0 |
very long chain acyl-coa dehydrogenase deficiency
|
mend syndrome
| 0 |
very long chain acyl-coa dehydrogenase deficiency
|
hypolipoproteinemia
| 0 |
very long chain acyl-coa dehydrogenase deficiency
|
ck syndrome
| 0 |
very long chain acyl-coa dehydrogenase deficiency
|
carnitine palmitoyltransferase ii deficiency
| 0 |
very long chain acyl-coa dehydrogenase deficiency
|
refsum disease
| 0 |
very long chain acyl-coa dehydrogenase deficiency
|
chylomicron retention disease
| 0 |
very long chain acyl-coa dehydrogenase deficiency
|
multiple congenital anomalies-hypotonia-seizures syndrome
| 0 |
very long chain acyl-coa dehydrogenase deficiency
|
carnitine palmitoyltransferase i deficiency
| 0 |
very long chain acyl-coa dehydrogenase deficiency
|
steroid inherited metabolic disorder
| 0 |
clivus chondroid chordoma
|
clivus chordoma
| 1 |
clivus chondroid chordoma
|
peho syndrome
| 0 |
clivus chondroid chordoma
|
alkuraya-kucinskas syndrome
| 0 |
clivus chondroid chordoma
|
parkinson's disease 22
| 0 |
clivus chondroid chordoma
|
visual verbal agnosia
| 0 |
clivus chondroid chordoma
|
basan syndrome
| 0 |
clivus chondroid chordoma
|
gallbladder cancer
| 0 |
clivus chondroid chordoma
|
amyotrophic lateral sclerosis type 13
| 0 |
clivus chondroid chordoma
|
murray valley encephalitis
| 0 |
clivus chondroid chordoma
|
nonsyndromic congenital nail disorder 3
| 0 |
clivus chondroid chordoma
|
lung hilum cancer
| 0 |
hellp syndrome
|
severe pre-eclampsia
| 1 |
hellp syndrome
|
autosomal dominant nonsyndromic deafness 3a
| 0 |
hellp syndrome
|
spastic ataxia
| 0 |
hellp syndrome
|
psychotic disorder
| 0 |
hellp syndrome
|
holoprosencephaly 3
| 0 |
hellp syndrome
|
doyne honeycomb retinal dystrophy
| 0 |
hellp syndrome
|
spinal muscular atrophy with lower extremity predominant
| 0 |
hellp syndrome
|
alpha-methylacyl-coa racemase deficiency
| 0 |
hellp syndrome
|
mesenchymoma
| 0 |
hellp syndrome
|
acute pulmonary heart disease
| 0 |
hellp syndrome
|
burkitt lymphoma
| 0 |
meier-gorlin syndrome 4
|
meier-gorlin syndrome
| 1 |
meier-gorlin syndrome 4
|
meier-gorlin syndrome 1
| 0 |
meier-gorlin syndrome 4
|
meier-gorlin syndrome 7
| 0 |
meier-gorlin syndrome 4
|
meier-gorlin syndrome 2
| 0 |
meier-gorlin syndrome 4
|
meier-gorlin syndrome 8
| 0 |
meier-gorlin syndrome 4
|
meier-gorlin syndrome 3
| 0 |
meier-gorlin syndrome 4
|
meier-gorlin syndrome 5
| 0 |
meier-gorlin syndrome 4
|
meier-gorlin syndrome 6
| 0 |
meier-gorlin syndrome 4
|
bilateral parasagittal parieto-occipital polymicrogyria
| 0 |
meier-gorlin syndrome 4
|
childhood intracortical osteosarcoma
| 0 |
meier-gorlin syndrome 4
|
schopf-schulz-passarge syndrome
| 0 |
benign epilepsy with centrotemporal spikes
|
childhood electroclinical syndrome
| 1 |
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