| 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 |