All terms in DOID

Label Id Description
obsolete Proteus infectious disease DOID_3881
obsolete anosognostic epilepsy DOID_2551
granulomatous angiitis DOID_2555
relapsing polychondritis DOID_2556 [A chondromalacia that is characterized by recurrent inflammation of cartilage and other tissues throughout the body.]
paranoid schizophrenia DOID_1229 [A schizophrenia characterized by delusions or auditory hallucinations of persecution or being plotted against without thought disorder, disorganized behavior, or affective flattening.]
infantile onset multisystem autoimmune disease 1 DOID_0061160 [An infantile onset multisystem autoimmune disease characterized by early childhood onset of a spectrum of autoimmune disorders affecting multiple organs that has_material_basis_in heterozygous gain of function mutation in the STAT3 gene on chromosome 17q21.]
obsolete paranoid type schizophrenia in remission DOID_1228
obsolete acute erythremia and erythroleukemia in remission DOID_1238
pustular psoriasis susceptibility 15 MIM_616106
fetishism DOID_1235
gender incongruence DOID_1234 [A sexual health disorder that involves a conflict between a person's actual physical gender and the gender that person identifies himself or herself as.]
transvestism DOID_1233
obsolete paranoid type schizophrenia subchronic state with acute exacerbation DOID_1232
obsolete chronic schizophrenia DOID_1231
Kariminejad neurodevelopmental syndrome DOID_0061158 [An autosomal recessive intellectual developmental disorder characterized by global developmental delay with delayed walking by a few years, speech delay, and impaired intellectual development that has_material_basis_in homozygous mutation in the RBSN gene on chromosome 3p25.]
familial isolated hypoparathyroidism 1 DOID_0061150 [A familial isolated hypoparathyroidism that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in the parathyroid hormone PTH gene on chromosome 11p15.]
familial isolated hypoparathyroidism 2 DOID_0061151 [A familial isolated hypoparathyroidism that has_material_basis_in homozygous mutation in the glial cells missing transcription factor-2 GCM2 gene on chromosome 6p24. Some patients have been reported with heterozygous mutations in the GCM2 gene.]
monilethrix 2 DOID_0061152 [A hair disease that is characterized by a 'beaded' appearance of affected hairs on microscopy, caused by elliptical nodes of normal thickness alternating with narrow, dystrophic constrictions and that has_material_basis_in heterozygous mutation in the KRT81 gene on chromosome 12q13.]
susceptibility to anorexia nervosa MIM_606788
monilethrix 3 DOID_0061153 [A hair disease that is characterized by periodic narrowing ('beading') along the hair shaft visible on microscopy and that has_material_basis_in heterozygous mutation in the KRT83 gene on chromosome 12q13.]