| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| STING-associated vasculopathy with onset in infancy |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Hakuri |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Bile acid coenzyme A ligase deficiency and defective amidation |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Papular mucinosis of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Non-Wilsonian hepatic copper toxicosis of infancy and childhood |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
4 |
| Entire life |
Is a |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
|
| Fatal infantile cytochrome C oxidase deficiency |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile striatonigral degeneration |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Behr syndrome |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Moyamoya disease with early onset achalasia |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Self-healing collodion baby |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
|
| Acral self-healing collodion baby |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
|
| Benign paroxysmal torticollis of infancy |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
3 |
| Infantile viral gastroenteritis |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile viral gastroenteritis |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Developmental delay, epilepsy, neonatal diabetes syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile dystonia parkinsonism |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infant gastrointestinal regurgitation |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Infant dyschezia |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile onset spinocerebellar ataxia |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
3 |
| Infantile onset spinocerebellar ataxia |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
4 |
| Infantile choroidocerebral calcification syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infant epilepsy with migrant focal crisis |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Permanent neonatal diabetes mellitus with cerebellar agenesis syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
4 |
| Whiplash shaken infant syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Apnea of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
5 |
| Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
|
| Erythroderma in infancy |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Severe myoclonic epilepsy in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Idiopathic hypercalcemia of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Infantile hypercalcemia |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Idiopathic infantile hypercalcemia - mild form |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Severe idiopathic hypercalcemia of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Allergic colitis caused by food protein in infant |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Allergic proctitis caused by food protein in infant |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
3 |
| Transient infantile hyperthyrotropinemia |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
3 |
| Underweight in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Nutritional wasting in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Acute malnutrition in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Nutritional stunting in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
|
| Infantile poisoning caused by mercury |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile stiff skin syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Benign infantile seizure with mild gastroenteritis syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Benign infantile seizure with mild gastroenteritis syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
3 |
| Benign infantile seizure with mild gastroenteritis syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Constantly crying infant |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Melanotic neuroectodermal tumor of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Syntaxin binding protein 1 encephalopathy with epilepsy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile hydrocele |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile gastroenteritis |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile gastroenteritis |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Nonbacterial gastroenteritis of infant |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Nonbacterial gastroenteritis of infant |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Benign partial epilepsy of infancy with complex partial seizures |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Benign infantile focal epilepsy with midline spikes and waves during sleep |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Benign partial epilepsy with secondarily generalized seizures in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Charcot-Marie-Tooth disease type 2B5 |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal recessive infantile hypercalcemia |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Laminin subunit beta 2 related infantile-onset nephrotic syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile autism |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Active infantile autism |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Residual infantile autism |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile onset panniculitis with uveitis and systemic granulomatosis |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile onset panniculitis with uveitis and systemic granulomatosis |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
3 |
| Infantile onset panniculitis with uveitis and systemic granulomatosis |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Transient infantile hypertriglyceridemia and hepatosteatosis |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Familial infantile gigantism |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Acute infantile liver failure with multisystemic involvement syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| FAST kinase domains 2-related infantile mitochondrial encephalomyopathy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| FAST kinase domains 2-related infantile mitochondrial encephalomyopathy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Chronic infantile eczema |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Desmoplastic infantile astrocytoma and ganglioglioma |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
3 |
| Fatal infantile hypertonic myofibrillar myopathy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile cerebellar and retinal degeneration |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile cerebellar and retinal degeneration |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Infantile cerebellar and retinal degeneration |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
3 |
| Malignant migrating partial seizures of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Familial infantile myoclonic epilepsy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile-onset autosomal recessive non progressive cerebellar ataxia |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile cataract |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Urticaria pigmentosa, infantile form |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Obesity due to SIM bHLH transcription factor 1 deficiency |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
4 |
| Acute infantile eczema |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| High risk infant |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Infantile acne |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Galactocerebroside beta-galactosidase deficiency - early onset |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Galactocerebroside beta-galactosidase deficiency - early onset |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Michelin-tire baby |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Refractory infantile spasms co-occurrent with status epilepticus |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Refractory infantile spasms co-occurrent with status epilepticus |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
2 |
| Mental disorder in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Persistent hyperinsulinemic hypoglycemia of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |
| Infantile idiopathic scoliosis of cervical spine |
Occurrence |
False |
Infancy |
Inferred relationship |
Existential restriction modifier |
1 |