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Metadata
ID	HP:0003593
Name	Infantile onset
Definition	Onset of signs or symptoms of disease between 28 days to one year of life.
Parent Relationships	is_a Pediatric onset is_a onset
Related Diseases	null immunodeficiency 95 immunodeficiency 96 immunodeficiency 106 immunodeficiency 116 severe combined immunodeficiency 124 immunodeficiency 128 hereditary spastic paraplegia 87 hereditary spastic paraplegia 88 hereditary spastic paraplegia 89 early-onset epilepsy 2 early-onset epilepsy 3 rhabdoid tumor predisposition syndrome acute myeloid leukemia with CBFA2T3-GLIS2 fusion existence starts during West syndrome arterial calcification of infancy infancy electroclinical syndrome infantile-onset myofibrillar myopathy 12 with cardiomyopathy benign familial infantile epilepsy immunodeficiency 81 immunodeficiency 94 immunodeficiency 100 severe combined immunodeficiency 105 immunodeficiency 114 immunodeficiency 115 immunodeficiency 118 immunodeficiency 122 infantile-onset distal myopathy hereditary spastic paraplegia 70 mitochondrial complex V (ATP synthase) deficiency nuclear type 4A X-linked mental retardation Gustavson type DeSanto-Shinawi syndrome desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma infant-type hemispheric glioma oxoglutarate dehydrogenase deficiency glycogen storage disease I neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities severe combined immunodeficiency 104 torsion dystonia with onset in infancy nemaline myopathy 5A STING-associated vasculopathy with onset in infancy Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome leucine-sensitive hypoglycemia of infancy neonatal diabetes mellitus progeria transient hypogammaglobulinemia of infancy has material basis in classic dopamine transporter deficiency syndrome infantile parkinsonism-dystonia 2