All terms in DOID

Label Id Description
eccrine sweat gland neoplasm DOID_173
Hexapoda NCBITaxon_6960
Pancrustacea NCBITaxon_197562
obsolete vulvar soft tissue tumor DOID_2083
obsolete vulvar blue nevus DOID_2085
obsolete blue nevus DOID_2086
obsolete outlet dysfunction constipation DOID_2088
obsolete constipation DOID_2089 [A bowel dysfunction that is characterized by infrequent or difficult evacuation of feces.]
Abnormality of skin pigmentation HP_0001000
Abnormal skin morphology HP_0011121
Abnormal cerebellar vermis morphology HP_0002334
Abnormal cerebellum morphology HP_0001317
megacystis-microcolon-intestinal hypoperistalsis syndrome DOID_0060610 [A syndrome that is characterized by marked dilatation of the bladder and microcolon and decreased intestinal peristalsis.]
abdominal obesity-metabolic syndrome DOID_0060611 [A syndrome that is characterized by abdominal obesity, blood lipid disorders, inflammation, insulin resistance or full-blown diabetes, and increased risk of developing cardiovascular disease.]
abdominal obesity-metabolic syndrome 3 DOID_0060612 [An abdominal obesity-metabolic syndrome that has_material_basis_in heterozygous mutation in the DYRK1B gene on chromosome 19q13.]
X-linked cleft palate with or without ankyloglossia DOID_0060613 [A cleft palate that has_material_basis_in mutation in the TBX22 gene on chromosome Xq21.]
cleft palate DOID_674 [An orofacial cleft characterized by a fissure of the soft and/or hard palate, due to faulty fusion of the two plates of the skull that form the hard palate.]
X-linked monogenic disease DOID_0050735 [A monogenic disease that has_material_basis_in mutations in genes on the X chromosome.]
ulnar-mammary syndrome DOID_0060614 [A syndrome that is characterized by posterior limb deficiencies or duplications, apocrine/mammary gland hypoplasia and, or dysfunction, abnormal dentition, delayed puberty in males, and genital anomalies and that has_material_basis_in heterozygous mutation in the TBX3 gene.]
Acariformes NCBITaxon_6946