Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Autosomal recessive infantile hypercalcaemia |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
LAMB2-related infantile-onset nephrotic syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Infantile autism |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Active infantile autism |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Residual infantile autism |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Infantile onset panniculitis with uveitis and systemic granulomatosis |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Infantile onset panniculitis with uveitis and systemic granulomatosis |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
3 |
Infantile onset panniculitis with uveitis and systemic granulomatosis |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Transient infantile hypertriglyceridaemia and hepatosteatosis |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
Familial infantile gigantism |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Acute infantile liver failure with multisystemic involvement syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
FAST kinase domains 2-related infantile mitochondrial encephalomyopathy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
FAST kinase domains 2-related infantile mitochondrial encephalomyopathy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
Chronic infantile eczema |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Desmoplastic infantile astrocytoma and ganglioglioma |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
3 |
Fatal infantile hypertonic myofibrillar myopathy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Infantile cerebellar and retinal degeneration |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Infantile cerebellar and retinal degeneration |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
Infantile cerebellar and retinal degeneration |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
3 |
Malignant migrating partial seizures of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Familial infantile myoclonic epilepsy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Infantile-onset autosomal recessive non progressive cerebellar ataxia |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Infantile cataract |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Urticaria pigmentosa, infantile form |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Obesity due to SIM1 deficiency |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
1 |
Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
4 |
Acute infantile eczema |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
High risk infant |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
Infantile acne |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Galactocerebroside beta-galactosidase deficiency - early onset |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Galactocerebroside beta-galactosidase deficiency - early onset |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
Michelin-tyre baby |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Refractory infantile spasms co-occurrent with status epilepticus |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Refractory infantile spasms co-occurrent with status epilepticus |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
Mental disorder in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Congenital hyperinsulinism |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Infantile idiopathic scoliosis of cervical spine |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
1 |
Infantile breast hypertrophy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Refractory infantile spasms |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
Refractory infantile spasms |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Fibrous hamartoma of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Cradle cap |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Generalised seborrhoeic dermatitis of infants |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Benign paroxysmal torticollis of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Infantile onset spinocerebellar ataxia |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Infantile onset spinocerebellar ataxia |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
Pelizaeus-Merzbacher disease, classic form |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
Pelizaeus-Merzbacher disease, classic form |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Infantile eczema |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Excessive crying of infant |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
X-linked acrogigantism due to Xq26 microduplication |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
4 |
Idiopathic hepatitis in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Sclerema neonatorum |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
Acropustulosis of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
Reactive attachment disorder of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Miliaria crystallina, infantile |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Miliaria crystallina, infantile |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
Underactive infant |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
Benign extra-axial hygroma |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Infantile pustular psoriasis |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Infantile pustular psoriasis |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
STING-associated vasculopathy with onset in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Warts of perianal region in infancy caused by human papillomavirus |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Salt-wasting syndrome of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Congenital esotropia |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Esotropia with dissociated vertical deviation |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Esotropia with nystagmus |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Esotropia with nystagmus block |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Bilateral congenital esotropia of eyes |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Bilateral congenital esotropia of eyes |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
Congenital esotropia of right eye |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Congenital esotropia of left eye |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Infantile haemangioma of subglottis |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
1 |
Sporadic infantile bilateral striatal necrosis |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Segmental infantile haemangioma |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Propriospinal myoclonus at sleep onset in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Erythroderma in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Infantile systemic hyalinosis |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
1 |
Infantile systemic hyalinosis |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
2 |
Infantile systemic hyalinosis |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
3 |
Aggressive infantile fibromatosis |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Infantile digital fibromatosis |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
Miliaria rubra, infantile |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Idiopathic arterial calcification of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Acquired iron deficiency anaemia due to increased requirement in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
3 |
Infant behaviour alteration |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
Infantile fucosidosis |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Infantile glycine encephalopathy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Juvenile polyposis of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Infantile posthaemorrhagic hydrocephalus |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Maternally inherited Leigh syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
3 |
Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
IL21-related infantile inflammatory bowel disease |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
Infantile inflammatory bowel disease with neurological involvement |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |