Visualize Submit Comment
Metadata
ID HP:0011463
Name Childhood onset
Definition Onset of disease at the age of between 1 and 5 years.
Parent Relationships

is_a Pediatric onset

is_a onset

Related Diseases

null

  • hereditary spastic paraplegia 87
  • hereditary spastic paraplegia 88
  • hereditary spastic paraplegia 89
  • early-onset epilepsy 2
  • early-onset epilepsy 3
  • existence starts during

  • intermediate spinal muscular atrophy
  • Lennox-Gastaut syndrome
  • alternating hemiplegia of childhood
  • childhood electroclinical syndrome
  • early onset absence epilepsy
  • childhood spinal muscular atrophy
  • myoclonic-atonic epilepsy
  • lymphoproliferative syndrome 1
  • childhood hepatocellular carcinoma
  • childhood acute myeloid leukemia
  • systemic Epstein-Barr virus positive T-cell lymphoma of childhood
  • malignant childhood adrenal gland pheochromocytoma
  • stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
  • childhood acute lymphocytic leukemia
  • childhood T-cell acute lymphoblastic leukemia
  • childhood B-cell acute lymphoblastic leukemia
  • T-cell childhood lymphoblastic lymphoma
  • spinal muscular atrophy type 0
  • childhood acute megakaryoblastic leukemia
  • childhood-onset asthma
  • childhood low-grade glioma
  • childhood supratentorial embryonal tumor with multilayered rosettes, C19MC-altered
  • spastic paraplegia with deafness
  • DeSanto-Shinawi syndrome
  • agammaglobulinemia 10
  • agammaglobulinemia 8B
  • cerebellar atrophy, visual impairment, and psychomotor retardation
  • Nestor-Guillermo progeria syndrome
  • Paget's disease of bone 2
  • disabling pansclerotic morphea
  • nemaline myopathy 5B
  • neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities
  • childhood sarcoma with BCOR genetic alterations
  • childhood round cell sarcoma with EWSR1-non-ETS fusion
  • childhood renal cell carcinoma with MiT translocations
  • childhood-onset dystonia with optic atrophy and basal ganglia abnormalities
  • PFAPA syndrome
  • progressive pseudorheumatoid arthropathy of childhood
  • glucose transporter type 1 deficiency syndrome 2
  • neuronal ceroid lipofuscinosis 6A
  • childhood hypophosphatasia
  • Werdnig-Hoffmann disease
  • childhood disintegrative disease
  • childhood type dermatomyositis
  • childhood absence epilepsy
  • Landau-Kleffner syndrome
  • childhood astrocytic tumor
  • childhood oligodendroglioma
  • Tay-Sachs disease
  • benign epilepsy with centrotemporal spikes
  • childhood osteosarcoma
  • childhood fibrosarcoma
  • childhood choroid plexus cancer
  • childhood spinal cord tumor
  • rhabdoid cancer
  • kidney rhabdoid cancer
  • childhood kidney cancer
  • childhood medulloblastoma
  • childhood central nervous system embryonal tumor
  • progeria
  • childhood brain stem neoplasm
  • childhood infratentorial neoplasm
  • childhood kidney cell carcinoma
  • childhood angiosarcoma
  • childhood mesenchymal chondrosarcoma
  • childhood meningioma
  • childhood mediastinal neurogenic tumor
  • pilomyxoid astrocytoma
  • pilocytic astrocytoma
  • childhood cerebellar neoplasm
  • childhood endodermal sinus tumor
  • childhood ependymoma
  • childhood liposarcoma
  • childhood parosteal osteogenic sarcoma
  • childhood lymphoma
  • childhood malignant mesenchymoma
  • central nervous system childhood germ cell tumor
  • childhood germ cell cancer
  • childhood testicular germ cell tumor
  • childhood ovarian endodermal sinus tumor
  • childhood ovarian germ cell tumor
  • childhood leptomeningeal melanoma
  • childhood choriocarcinoma of the testis
  • childhood testicular mixed germ cell tumor
  • childhood embryonal testis carcinoma
  • childhood mature teratoma of the ovary
  • childhood teratoma of the ovary
  • childhood cerebellar astrocytic neoplasm
  • childhood brain stem glioma
  • childhood brainstem astrocytoma
  • childhood central nervous system mature teratoma
  • childhood teratocarcinoma of the testis
  • childhood myxoid chondrosarcoma
  • childhood optic tract astrocytoma
  • childhood optic nerve glioma
  • childhood CNS choriocarcinoma
  • childhood central nervous system immature teratoma
  • childhood botryoid rhabdomyosarcoma
  • childhood vagina botryoid rhabdomyosarcoma
  • vulvar childhood botryoid-type embryonal rhabdomyosarcoma
  • juvenile pilocytic astrocytoma
  • childhood pilocytic astrocytoma
  • childhood intraocular retinoblastoma
  • childhood brain meningioma
  • childhood cerebral astrocytoma
  • childhood immature teratoma of ovary
  • childhood epithelioid sarcoma
  • childhood CNS embryonal cell carcinoma
  • childhood extraosseous osteosarcoma
  • childhood ovarian dysgerminoma
  • childhood brain germinoma
  • childhood germ cell brain tumor
  • childhood pleomorphic rhabdomyosarcoma
  • childhood infratentorial ependymoma
  • childhood supratentorial ependymoma
  • childhood central nervous system mixed germ cell tumor
  • childhood infratentorial embryonal tumor with multilayered rosettes, C19MC-altered
  • childhood intracortical osteosarcoma
  • childhood malignant hemangiopericytoma
  • childhood malignant schwannoma
  • childhood extraocular retinoblastoma
  • childhood leukemia
  • childhood multilocular cystic kidney neoplasm
  • childhood embryonal tumor with multilayered rosettes, C19MC-altered
  • childhood ovarian embryonal carcinoma
  • childhood central nervous system germinoma
  • malignant childhood germ cell neoplasm
  • childhood choriocarcinoma of the ovary
  • childhood kidney angiomyolipoma
  • congenital fibrosarcoma
  • Add an item to the term tracker