| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Infantile idiopathic scoliosis of cervical spine |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile breast hypertrophy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Refractory infantile spasms |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Refractory infantile spasms |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Fibrous hamartoma of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Cradle cap |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Generalized seborrheic dermatitis of infants |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Benign paroxysmal torticollis of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile onset spinocerebellar ataxia |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile onset spinocerebellar ataxia |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Pelizaeus-Merzbacher disease, classic form |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Pelizaeus-Merzbacher disease, classic form |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile eczema |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Excessive crying of infant |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| X-linked acrogigantism due to Xq26 microduplication |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
4 |
| Idiopathic hepatitis in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Sclerema neonatorum |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Acropustulosis of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Reactive attachment disorder of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Miliaria crystallina, infantile |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Miliaria crystallina, infantile |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Underactive infant |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Benign extra-axial hygroma |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile pustular psoriasis |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile pustular psoriasis |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| STING-associated vasculopathy with onset in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Warts of perianal region in infancy caused by human papillomavirus |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Salt-wasting syndrome of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile esotropia |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Esotropia with dissociated vertical deviation |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Esotropia with nystagmus |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Esotropia with nystagmus block |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile esotropia of bilateral eyes |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile esotropia of bilateral eyes |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Infantile esotropia of right eye |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile esotropia of left eye |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile hemangioma of subglottis |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Sporadic infantile bilateral striatal necrosis |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Segmental infantile hemangioma |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Propriospinal myoclonus at sleep onset in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Erythroderma in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile systemic hyalinosis |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile systemic hyalinosis |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Infantile systemic hyalinosis |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
3 |
| Aggressive infantile fibromatosis |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile digital fibromatosis |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Miliaria rubra, infantile |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Idiopathic arterial calcification of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Iron deficiency anemia due to increased requirement in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
3 |
| Infant behavior alteration |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Infantile fucosidosis |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile glycine encephalopathy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Juvenile polyposis of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile posthemorrhagic hydrocephalus |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Maternally inherited Leigh syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
3 |
| Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Interleukin 21 related infantile inflammatory bowel disease |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile inflammatory bowel disease with neurological involvement |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Intellectual disability, epilepsy, extrapyramidal syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Intellectual disability, epilepsy, extrapyramidal syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Intellectual disability, epilepsy, extrapyramidal syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
3 |
| Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
3 |
| Infantile pyknocytosis |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinemia |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Periodic fever, infantile enterocolitis, autoinflammatory syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Periodic fever, infantile enterocolitis, autoinflammatory syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
3 |
| Functional constipation of infants |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Familial infantile bilateral striatal necrosis |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Fever-associated acute infantile liver failure syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Laminin subunit alpha 5-related multisystemic syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
3 |
| Benign familial neonatal-infantile seizures |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Benign familial infantile epilepsy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Toilet trained |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Finding of infant milestone |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Impairment of infant development |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Impairment of newborn development |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile pedal papules |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile impetiginized atopic dermatitis |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Alexander disease infantile form |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Alexander disease infantile form |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Alexander disease infantile form |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
4 |
| Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
6 |
| Infantile multisystem neurologic, endocrine, pancreatic disease |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile multisystem neurologic, endocrine, pancreatic disease |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Infantile multisystem neurologic, endocrine, pancreatic disease |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
3 |
| Infantile seborrheic dermatitis NOS (disorder) |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
|
| Other nonsenile cataract |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
|
| Nonsenile cataract NOS |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
|
| Sudden infant death syndrome with mention of autopsy |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
|
| Sudden infant death syndrome without mention of autopsy |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
|