| 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 |