All terms in DOID

Label Id Description
obsolete lentiginosis profusa DOID_0050531
intermediate spinal muscular atrophy DOID_0050530 [A childhood spinal muscular atrophy that is characterized by progressive muscular weakness and respiratory failure, develops in children between the ages of 6 and 12 months and drastically reduces length of life, and has_material_basis_in mutations in the SMN1 or SMN2 genes that are required for the survival of motor neurons.]
Angiostrongylus NCBITaxon_6312
Metastrongylidae NCBITaxon_55271
Mumps orthorubulavirus NCBITaxon_2560602
obsolete soldiers heart DOID_0050533
obsolete epidermal nevus DOID_0050532
congenital stationary night blindness DOID_0050534 [A hereditary night blindness that is characterized by hemeralopia with a moderate loss of visual acuity and caused by defective photoreceptor-to-bipolar cell signaling with common ERG findings of reduced or absent b-waves and generally normal a-waves.]
posterior polar cataract DOID_0050537 [A cataract that is characterized by a distinctive discoid lens opacity situated posteriorly and adjacent to the posterior capsule.]
obsolete SC phocomelia syndrome DOID_0050536 [A syndrome that is characterized by severe prenatal growth retardation resulting in malformation of the bones in the skull, face and limbs, has_material_basis_in the mutation in the ESCO2 gene.]
obsolete Lymphocytic choriomeningitis virus meningoencephalitis DOID_0050520 [A lymphocytic choriomeningitis that results_in inflammation located_in meninges and located_in brain, has_material_basis_in Lymphocytic choriomeningitis virus, which is transmitted_by common house mouse, Mus musculus. The infection has_symptom fever, has_symptom headache, has_symptom stiff neck, has_symptom drowsiness, has_symptom confusion, has_symptom sensory disturbances, and has_symptom paralysis.]
gene SO_0000704
adult spinal muscular atrophy DOID_0050529 [A spinal muscular atrophy that is characterized by progressive muscular weakness and motor disability that typically presents in the third decade of life and has_material_basis_in mutations in the SMN1 or SMN2 genes that are required for the survival of motor neurons.]
Balkan hemorrhagic fever DOID_0050522 [A hemorrhagic fever with renal syndrome that results in infection located in kidney, has_material_basis_in Dobrava-Belgrade virus (Orthohantavirus dobravaense), which is transmitted by yellow-necked field mouse, Apodemus flavicollis. The infection has symptom headache, has symptom fever, has symptom muscle pains, has symptom facial flush, has symptom petechiae, has symptom proteinuria, and has symptom renal failure.]
Oropouche fever DOID_0050521 [A viral infectious disease that results in infection, has_material_basis_in Oropouche virus (Orthobunyavirus oropoucheense), which is transmitted by biting midge, Culicoides paraensis. The infection has symptom fever, has symptom chills, has symptom headache, has symptom anorexia, has symptom muscle pain, has symptom joint pain, and has symptom vomiting.]
asbestos CHEBI_46661 [Fibrous incombustible mineral composed of magnesium and calcium silicates with or without other elements.]
adult T-cell leukemia/lymphoma DOID_0050523 [A T-cell acute leukemia that results_in abnormal increase of lymphocytes, derives_from T-cells, has_material_basis_in human T-cell leukemia virus type 1 (Deltaretrovirus priTlym1), which is transmitted_by sexual contact, transmitted_by contaminated needles used by intravenous-drug users, and transmitted_by breast feeding. The infection results_in_formation_of skin lesions.]
Gamstorp-Wohlfart syndrome DOID_0050526 [A syndrome characterized by progressive weakness and atrophy of muscles in feet, legs and hands. In some patients the syndrome also causes decreased sensitivity to touch, heat or cold, particularly in the lower arms or legs.]
obsolete acroosteolysis DOID_0050525
nonphotosensitive trichothiodystrophy 4 DOID_0050528 [A nonphotosensitive trichothiodystrophy that is characterized by brittle hair, short stature, decreased fertility and cognitive impairment without photosensitivity has_material_basis_in mutations in the TTDN1 gene.]