From birth to adulthood without peak of onset.
This is just here as a test because I lose it
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- Familial generalized lentiginosis
- Hepatitis delta
- Familial dysfibrinogenemia
- Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome
- Optic pathway glioma
- Congenital dyserythropoietic anemia type III
- Langerhans cell sarcoma
- Nodular lymphocyte predominant Hodgkin lymphoma
- Diffuse intrinsic pontine glioma
- Pseudohypoparathyroidism
- Unclassified myelodysplastic syndrome
- Acute leukemia of ambiguous lineage
- Myeloid sarcoma
- Chronic primary adrenal insufficiency
- Thrombomodulin-related bleeding disorder
- Subcutaneous panniculitis-like T-cell lymphoma
- Southeast Asian ovalocytosis
- Hereditary thrombocytopenia with normal platelets
- Benign adult familial myoclonic epilepsy
- Mast cell leukemia
- Anaplastic large cell lymphoma
- Lymphomatoid papulosis
- Acute myeloblastic leukemia with maturation
- Therapy related acute myeloid leukemia and myelodysplastic syndrome
- Cat-scratch disease
- Arachnoiditis
- Methylmalonic acidemia without homocystinuria
- Primary cutaneous amyloidosis
- Heparin-induced thrombocytopenia
- Essential thrombocythemia
- Zika virus disease
- Fibrosarcoma
- Filariasis
- Lymphatic filariasis
- Hereditary gingival fibromatosis
- Mounier-Kühn syndrome
- Glomus tumor
- Eosinophilic gastroenteritis
- African trypanosomiasis
- American trypanosomiasis
- Essential fructosuria
- Tuberculosis
- Tularemia
- Foix-Chavany-Marie syndrome
- Coronary arterial fistula
- Familial cerebral saccular aneurysm
- Rare hereditary hemochromatosis
- Acquired hemophagocytic lymphohistiocytosis associated with malignant disease
- Drug-induced lupus erythematosus
- Acute motor and sensory axonal neuropathy
- Acute motor axonal neuropathy
- Acute inflammatory demyelinating polyradiculoneuropathy
- Miller Fisher syndrome
- Fleck corneal dystrophy
- Macular corneal dystrophy
- Schnyder corneal dystrophy
- Lattice corneal dystrophy type I
- Follicular dendritic cell sarcoma
- Familial primary localized cutaneous amyloidosis
- Hartnup disease
- Guillain-Barré syndrome
- Vogt-Koyanagi-Harada disease
- Nodular neuronal heterotopia
- Hereditary xanthinuria
- Hemoglobin C disease
- Hemoglobin E disease
- Atypical hemolytic uremic syndrome
- Solitary fibrous tumor/hemangiopericytoma
- Kaposiform hemangioendothelioma
- Anti-HLA hyperimmunization
- Hemophagocytic syndrome associated with an infection
- Methylcobalamin deficiency type cblG
- Generalized juvenile polyposis/juvenile polyposis coli
- Complex regional pain syndrome type 2
- Complex regional pain syndrome type 1
- Idiopathic multicentric Castleman disease
- HHV-8-associated multicentric Castleman disease
- Classic neuroendocrine tumor of appendix
- Supravalvular aortic stenosis
- Idiopathic bronchiectasis
- Ricin poisoning
- Renal hypoplasia, bilateral
- Renal hypoplasia, unilateral
- Unilateral multicystic dysplastic kidney
- Streptococcal toxic-shock syndrome
- Staphylococcal toxic-shock syndrome
- Idiopathic disseminated cytomegalovirus infection
- Spheroid body myopathy
- Streptobacillary rat-bite fever
- Spirillary rat-bite fever
- Pulmonary alveolar microlithiasis
- Hereditary sensory and autonomic neuropathy type 1
- Paraneoplastic neurologic syndrome
- Argyria
- Posterior corneal dystrophy
- Superficial corneal dystrophy
- Stromal corneal dystrophy
- Chronic intestinal failure
- Acute generalized exanthematous pustulosis