All terms in DOID

Label Id Description
xeroderma pigmentosum DOID_0050427 [A syndrome that is characterized by a deficiency in the ability to repair ultraviolet damage that has_material_basis_in autosomal recessive inheritance of DNA repair.]
X-linked atrophic macular degeneration DOID_0112157 [A macular degeneration characterized by macular atrophy causing progressive loss of visual acuity with minimal peripheral visual impairment that has_material_basis_in hemizygous mutation in RPGR on chromosome Xp11.4.]
alcuronium bromide allergy DOID_0040077 [A drug allergy that has_allergic_trigger alcuronium bromide.]
phthalyl group allergy DOID_0040076 [A drug allergy that has_allergic_trigger phthalyl group.]
benzo[d]isothiazol-3-one allergic contact dermatitis DOID_0040075 [An allergic contact dermatitis that has_allergic_trigger benzo[d]isothiazol-3-one.]
formaldehyde allergic contact dermatitis DOID_0040074 [An allergic contact dermatitis that has_allergic_trigger formaldehyde.]
2,4-dinitrophenyl allergic contact dermatitis DOID_0040079 [An allergic contact dermatitis that has_allergic_trigger 2,4-dinitrophenyl group.]
gallamine allergy DOID_0040078 [A drug allergy that has_allergic_trigger gallamine.]
parathyroid glandular cell CL_1001593
epithelial cell of parathyroid gland CL_0002260
disodium cromoglycate allergy DOID_0040073 [A drug allergy that has_allergic_trigger disodium cromoglycate.]
parthenolide allergic contact dermatitis DOID_0040072 [An allergic contact dermatitis that has_allergic_trigger parthenolide.]
sodium aurothiomalate allergy DOID_0040071 [A drug allergy that has_allergic_trigger sodium aurothiomalate.]
pancreas exocrine glandular cell CL_1001599
exocrine cell CL_0000152
epithelial cell of exocrine pancreas CL_1001433
co-trimoxazole allergy DOID_0040070 [A drug allergy that has_allergic_trigger co-trimoxazole.]
hordeolum externum DOID_13134 [A blepharitis that is characterized by an infection of the sebaceous glands of Zeis at the base of the eyelashes, or an infection of the apocrine sweat glands of Moll.]
X-linked intellectual developmental disorder 109 DOID_0080984 [A syndromic X-linked intellectual disability characterized by mildly to moderately impaired intellectual development associated with learning difficulties, communication deficits, attention problems, hyperactivity, and autistic behavior and that has_material_basis_in disruption of the FMR2 gene (AFF2), either by expansion of a CCG repeat in the 5-prime untranslated region or by deletion.]
thyroid dyshormonogenesis 6 DOID_0112189 [A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in DUOX2 on chromosome 15q21.1.]