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 |