all ages
http://www.orpha.net/ORDO/Orphanet_409950
From birth to adulthood without peak of onset.
Term info
Term relations
Related from:
has_age_of_onset
- 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
- 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
- Indolent systemic mastocytosis
- 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
- Osteochondritis of tarsal/metatarsal bone
- African trypanosomiasis
- American trypanosomiasis
- Essential fructosuria
- Tuberculosis
- Tularemia
- Coronary arterial fistulas
- Familial cerebral saccular aneurysm
- Rare hereditary hemochromatosis
- Drug-induced lupus erythematosus
- Acute motor and sensory axonal neuropathy
- Acute motor axonal neuropathy
- Acute inflammatory demyelinating polyradiculoneuropathy
- Miller-Fisher syndrome
- Juvenile glaucoma
- 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
- Whipple disease
- Kaposiform hemangioendothelioma
- Anti-HLA hyperimmunization
- Methylcobalamin deficiency type cblG
- Generalized juvenile polyposis/juvenile polyposis coli
- Complex regional pain syndrome type 2
- Complex regional pain syndrome type 1
- Classic neuroendocrine tumor of appendix
- Supravalvular aortic stenosis
- Renal hypoplasia, bilateral
- Renal hypoplasia, unilateral
- Spheroid body myopathy
- Pulmonary alveolar microlithiasis
- Hereditary sensory and autonomic neuropathy type 1
- Paraneoplastic neurologic syndrome
- Posterior corneal dystrophy
- Superficial corneal dystrophy
- Stromal corneal dystrophy
- Chronic intestinal failure
- Acute generalized exanthematous pustulosis
- Familial intestinal malrotation
- Sarcosinemia
- Familial juvenile hyperuricemic nephropathy type 1
- Rotor syndrome
- VIPoma
- Insulinoma
- Spinocerebellar ataxia type 12
- Spinocerebellar ataxia type 17
- Spinocerebellar ataxia type 1
- Spinocerebellar ataxia type 2
- Hereditary amyloidosis with primary renal involement