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 |
|