| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| STING-associated vasculopathy with onset in infancy (disorder) |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
2 |
| Hakuri |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
1 |
| Bile acid coenzyme A ligase deficiency and defective amidation (disorder) |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
1 |
| Papular mucinosis of infancy (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
4 |
| Entire life |
Is a |
False |
Infancy |
Inferred relationship |
Some |
|
| Fatal infantile cytochrome C oxidase deficiency (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Infantile striatonigral degeneration (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Behr syndrome |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
1 |
| Moyamoya disease with early onset achalasia (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
| Self-healing collodion baby (disorder) |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
|
| Acral self-healing collodion baby (disorder) |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
|
| Benign paroxysmal torticollis of infancy (disorder) |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
3 |
| Infantile viral gastroenteritis |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Infantile viral gastroenteritis |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
| Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein (disorder) |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
2 |
| Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Infantile dystonia parkinsonism (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Infant gastrointestinal regurgitation (finding) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
| Infant dyschezia (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Infantile onset spinocerebellar ataxia (disorder) |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
3 |
| Infantile onset spinocerebellar ataxia (disorder) |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
4 |
| Infantile choroidocerebral calcification syndrome (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Infant epilepsy with migrant focal crisis (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
| Permanent neonatal diabetes mellitus with cerebellar agenesis syndrome (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
4 |
| Whiplash shaken infant syndrome (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
| Apnea of infancy (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
5 |
| Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
|
| Erythroderma in infancy |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
2 |
| Severe myoclonic epilepsy in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Idiopathic hypercalcemia of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
| Infantile hypercalcemia |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
| Idiopathic infantile hypercalcaemia - mild form |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
| Severe idiopathic hypercalcemia of infancy (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
| Food protein-induced colitis in infant |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
| Food protein-induced proctitis in infant |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
3 |
| Transient infantile hyperthyrotropinemia (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
3 |
| Underweight in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Nutritional wasting in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Acute malnutrition in infancy (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Nutritional stunting in infancy (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
|
| Infantile mercury poisoning |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Infantile stiff skin syndrome (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Benign infantile seizure with mild gastroenteritis syndrome (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
| Benign infantile seizure with mild gastroenteritis syndrome (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
3 |
| Benign infantile seizure with mild gastroenteritis syndrome (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Constantly crying infant (finding) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
| Melanotic neuroectodermal tumor of infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Syntaxin binding protein 1 encephalopathy with epilepsy (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Infantile hydrocele |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Infantile gastroenteritis |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Infantile gastroenteritis |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
| Nonbacterial gastroenteritis of infant |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
| Nonbacterial gastroenteritis of infant |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Benign partial epilepsy of infancy with complex partial seizures (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Benign infantile focal epilepsy with midline spikes and waves during sleep |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Benign partial epilepsy with secondarily generalised seizures in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Charcot-Marie-Tooth disease type 2B5 |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Autosomal recessive infantile hypercalcemia (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
| LAMB2-related infantile-onset nephrotic syndrome |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Infantile autism (disorder) |
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 (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Infantile onset panniculitis with uveitis and systemic granulomatosis (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
3 |
| Infantile onset panniculitis with uveitis and systemic granulomatosis (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
| Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Transient infantile hypertriglyceridemia and hepatosteatosis |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
| Familial infantile gigantism (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein (disorder) |
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 (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| FAST kinase domains 2-related infantile mitochondrial encephalomyopathy (disorder) |
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 (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Infantile cerebellar and retinal degeneration (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Infantile cerebellar and retinal degeneration (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
| Infantile cerebellar and retinal degeneration (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
3 |
| Malignant migrating partial seizures of infancy (disorder) |
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 (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Cutaneous mastocytosis, infantile form (disorder) |
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 (disorder) |
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 (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Refractory infantile spasms co-occurrent with status epilepticus (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
2 |
| Mental disorder in infancy |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Persistent hyperinsulinemic hypoglycemia of infancy (disorder) |
Occurrence |
True |
Infancy |
Inferred relationship |
Some |
1 |
| Infantile idiopathic scoliosis of cervical spine |
Occurrence |
False |
Infancy |
Inferred relationship |
Some |
1 |