All terms in DOID

Label Id Description
obsolete ocular tuberculosis DOID_233
obsolete iridodialysis DOID_239
obsolete adhesions and disruptions of iris and ciliary body DOID_237
Joubert syndrome with orofaciodigital defect DOID_0060376 [A Joubert syndrome that is characterized by orofaciodigital defect.]
orofaciodigital syndrome V DOID_0060375 [An orofaciodigital syndrome that is characterized by postaxial polydactyly and median cleft of the upper lip and has_material_basis_in homozygous mutation in the DDX59 gene on chromosome 1q32.]
orange food product FOODON_00002071
orofaciodigital syndrome IV DOID_0060374 [An orofaciodigital syndrome that is characterized by dysmorphic facies, the development of harmartomas of the tongue, polydactyly and limb dysplasia, has_material_basis_in autosomal recessive inheritance of mutations in the TCTN3 gene.]
cannabis dependence DOID_1849 [A drug dependence that involves the continued use of cannabis despite problems related to use of the substance.]
orofaciodigital syndrome III DOID_0060373 [An orofaciodigital syndrome that is characterized by dysmorphic facies and severe intellectual deficits, and has_material_basis_in autosomal recessive inheritance.]
Parkinson's disease 15 DOID_0060372 [An early-onset Parkinson's disease that has_material_basis_in mutation in the FBXO7 gene on chromosome 22q12.3.]
Parkinson's disease 8 DOID_0060371 [A late onset Parkinson's disease that has_material_basis_in heterozygous mutation in the dardarin encoding gene on chromosome 12q12.]
lateral sclerosis DOID_230 [A motor neuron disease characterized by painless but progressive weakness and stiffness of the muscles of the legs.]
pacific salmon food product FOODON_00002075
Parkinson's disease 7 DOID_0060370 [An early-onset Parkinson's disease that has_material_basis_in homozygous or compound heterozygous mutation in the DJ1 gene on chromosome 1p36.]
obsolete Strongylida infectious disease DOID_1845 [A Rhabditida infectious disease that involves parasitic infection of gastrointestinal tracts of ruminants, horses, cats, dogs, swine and humans by nematodes belonging to the suborder Strongylida.]
mononeuritis of upper limb DOID_1844
Parkinson's disease 6 DOID_0060369 [An early-onset Parkinson's disease that has_material_basis_in mutations in the PINK1 gene on chromosome 1p36.12.]
Parkinson's disease 2 DOID_0060368 [An early-onset Parkinson's disease that has_material_basis_in mutation in the parkin gene on chromosome 6q25.2-q27.]
Parkinson's disease 1 DOID_0060367 [A late onset Parkinson's disease that has_material_basis_in mutation in the alpha-synuclein gene on chromosome 4q22.1.]
Hennekam syndrome DOID_0060366 [A lymphatic system disease characterized by he presence of intestinal lymphangiectasia, mental retardation, and characteristic facial anomalies. It is inherited in an autosomal recessive pattern. Most individuals with Hennekam syndrome have characteristic facial abnormalities, such as a flat face with accompanying puffy eyelids and hypertelorism; the nasal bridge is typically flat and the ears are typically small. Congenital extremity and genital lymphedema is present in most patients.]