child
stringlengths 4
125
| parent
stringlengths 4
125
| label
int64 0
1
|
|---|---|---|
infantile cerebellar-retinal degeneration
|
secondary parkinson disease
| 0 |
infantile cerebellar-retinal degeneration
|
primary cerebellar degeneration
| 0 |
infantile cerebellar-retinal degeneration
|
plexopathy
| 0 |
infantile cerebellar-retinal degeneration
|
agenesis of the corpus callosum with peripheral neuropathy
| 0 |
infantile cerebellar-retinal degeneration
|
familial encephalopathy with neuroserpin inclusion bodies
| 0 |
neurogenic arthropathy
|
arthropathy
| 1 |
neurogenic arthropathy
|
hemarthrosis
| 0 |
neurogenic arthropathy
|
secondary hypertrophic osteoarthropathy
| 0 |
neurogenic arthropathy
|
behcet's syndrome arthropathy
| 0 |
neurogenic arthropathy
|
ankylosis
| 0 |
neurogenic arthropathy
|
spondyloarthropathy
| 0 |
neurogenic arthropathy
|
plica syndrome
| 0 |
neurogenic arthropathy
|
bursitis
| 0 |
neurogenic arthropathy
|
ganglion or cyst of synovium/tendon/bursa
| 0 |
neurogenic arthropathy
|
hydrarthrosis
| 0 |
neurogenic arthropathy
|
shoulder impingement syndrome
| 0 |
miliaria rubra
|
miliaria
| 1 |
miliaria rubra
|
miliaria profunda
| 0 |
miliaria rubra
|
miliaria crystallina
| 0 |
miliaria rubra
|
miliaria pustulosa
| 0 |
miliaria rubra
|
congenital adrenal insufficiency
| 0 |
miliaria rubra
|
mitochondrial complex iii deficiency nuclear type 6
| 0 |
miliaria rubra
|
alcohol-related neurodevelopmental disorder
| 0 |
miliaria rubra
|
neurocirculatory asthenia
| 0 |
miliaria rubra
|
primary autosomal recessive microcephaly 3
| 0 |
miliaria rubra
|
intracranial sinus thrombosis
| 0 |
miliaria rubra
|
viral esophagitis
| 0 |
isolated microphthalmia 7
|
isolated microphthalmia
| 1 |
isolated microphthalmia 7
|
isolated microphthalmia 5
| 0 |
isolated microphthalmia 7
|
isolated microphthalmia 3
| 0 |
isolated microphthalmia 7
|
isolated microphthalmia 1
| 0 |
isolated microphthalmia 7
|
isolated microphthalmia 6
| 0 |
isolated microphthalmia 7
|
isolated microphthalmia 2
| 0 |
isolated microphthalmia 7
|
isolated microphthalmia 4
| 0 |
isolated microphthalmia 7
|
isolated microphthalmia 8
| 0 |
isolated microphthalmia 7
|
spastic entropion
| 0 |
isolated microphthalmia 7
|
corticosterone methyloxidase deficiency 1
| 0 |
isolated microphthalmia 7
|
b cell and dendritic cell deficiency
| 0 |
spondyloepimetaphyseal dysplasia, genevieve-type
|
spondyloepimetaphyseal dysplasia
| 1 |
spondyloepimetaphyseal dysplasia, genevieve-type
|
dyggve-melchior-clausen disease
| 0 |
spondyloepimetaphyseal dysplasia, genevieve-type
|
schimke immuno-osseous dysplasia
| 0 |
spondyloepimetaphyseal dysplasia, genevieve-type
|
spondyloepimetaphyseal dysplasia, pakistani type
| 0 |
spondyloepimetaphyseal dysplasia, genevieve-type
|
spondylometaepiphyseal dysplasia, short limb-hand type
| 0 |
spondyloepimetaphyseal dysplasia, genevieve-type
|
anauxetic dysplasia
| 0 |
spondyloepimetaphyseal dysplasia, genevieve-type
|
metatropic dysplasia
| 0 |
spondyloepimetaphyseal dysplasia, genevieve-type
|
spondyloepimetaphyseal dysplasia with joint laxity
| 0 |
spondyloepimetaphyseal dysplasia, genevieve-type
|
spondyloepimetaphyseal dysplasia, sponastrime type
| 0 |
spondyloepimetaphyseal dysplasia, genevieve-type
|
x-linked spondyloepimetaphyseal dysplasia
| 0 |
spondyloepimetaphyseal dysplasia, genevieve-type
|
spondyloepimetaphyseal dysplasia, missouri type
| 0 |
intellectual disability-severe speech delay-mild dysmorphism syndrome
|
syndromic intellectual disability
| 1 |
intellectual disability-severe speech delay-mild dysmorphism syndrome
|
syndromic x-linked intellectual disability
| 0 |
intellectual disability-severe speech delay-mild dysmorphism syndrome
|
neurodevelopmental disorder with midbrain and hindbrain malformations
| 0 |
intellectual disability-severe speech delay-mild dysmorphism syndrome
|
developmental delay and seizures with or without movement abnormalities
| 0 |
intellectual disability-severe speech delay-mild dysmorphism syndrome
|
tatton-brown-rahman syndrome
| 0 |
intellectual disability-severe speech delay-mild dysmorphism syndrome
|
mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations
| 0 |
intellectual disability-severe speech delay-mild dysmorphism syndrome
|
kaufman oculocerebrofacial syndrome
| 0 |
intellectual disability-severe speech delay-mild dysmorphism syndrome
|
pitt-hopkins-like syndrome 2
| 0 |
intellectual disability-severe speech delay-mild dysmorphism syndrome
|
abdominal obesity-metabolic syndrome 3
| 0 |
intellectual disability-severe speech delay-mild dysmorphism syndrome
|
onchocerciasis
| 0 |
intellectual disability-severe speech delay-mild dysmorphism syndrome
|
intracranial sinus thrombosis
| 0 |
salpingo-oophoritis
|
oophoritis
| 1 |
salpingo-oophoritis
|
larynx sarcoma
| 0 |
salpingo-oophoritis
|
opportunistic mycosis
| 0 |
salpingo-oophoritis
|
ghosal hematodiaphyseal syndrome
| 0 |
salpingo-oophoritis
|
chronic atrial and intestinal dysrhythmia
| 0 |
salpingo-oophoritis
|
x-linked epilepsy with variable learning disabilities and behavior disorders
| 0 |
salpingo-oophoritis
|
iron metabolism disease
| 0 |
salpingo-oophoritis
|
anal paget's disease
| 0 |
salpingo-oophoritis
|
familial episodic pain syndrome 3
| 0 |
salpingo-oophoritis
|
epidural spinal canal meningioma
| 0 |
salpingo-oophoritis
|
classic congenital mesoblastic nephroma
| 0 |
adhesive otitis media
|
auditory system disease
| 1 |
adhesive otitis media
|
necrosis of ear ossicle
| 0 |
adhesive otitis media
|
nonsyndromic deafness
| 0 |
adhesive otitis media
|
otorrhea
| 0 |
adhesive otitis media
|
middle ear disease
| 0 |
adhesive otitis media
|
retrocochlear disease
| 0 |
adhesive otitis media
|
external ear disease
| 0 |
adhesive otitis media
|
inner ear disease
| 0 |
adhesive otitis media
|
dislocation of ear ossicle
| 0 |
adhesive otitis media
|
autosomal recessive intellectual developmental disorder 61
| 0 |
adhesive otitis media
|
mitral valve disease
| 0 |
neuronal intestinal dysplasia type b
|
intestinal pseudo-obstruction
| 1 |
neuronal intestinal dysplasia type b
|
autosomal dominant familial visceral neuropathy
| 0 |
neuronal intestinal dysplasia type b
|
neuronal intestinal dysplasia type a
| 0 |
neuronal intestinal dysplasia type b
|
x-linked chronic idiopathic intestinal pseudo-obstruction
| 0 |
neuronal intestinal dysplasia type b
|
cone-rod dystrophy 12
| 0 |
neuronal intestinal dysplasia type b
|
esophagus leiomyoma
| 0 |
neuronal intestinal dysplasia type b
|
cutaneous leishmaniasis
| 0 |
neuronal intestinal dysplasia type b
|
jaw-winking syndrome
| 0 |
neuronal intestinal dysplasia type b
|
congenital leptin deficiency
| 0 |
neuronal intestinal dysplasia type b
|
vasculitis
| 0 |
neuronal intestinal dysplasia type b
|
thymus mucoepidermoid carcinoma
| 0 |
parietal lobe ependymoma
|
parietal lobe neoplasm
| 1 |
parietal lobe ependymoma
|
lassa fever
| 0 |
parietal lobe ependymoma
|
non-syndromic x-linked intellectual disability 101
| 0 |
parietal lobe ependymoma
|
gallbladder papillary carcinoma
| 0 |
parietal lobe ependymoma
|
abducens nerve neoplasm
| 0 |
parietal lobe ependymoma
|
acute cervicitis
| 0 |
parietal lobe ependymoma
|
patent blue v allergy
| 0 |
Subsets and Splits
No community queries yet
The top public SQL queries from the community will appear here once available.