Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
metatypical basal cell carcinoma	DOID_4281	[A basal cell carcinoma characterized by intermediate typology between basal cell carcinoma and squamous cell carcinoma.]
anal margin basal cell carcinoma	DOID_4283	[A basal cell carcinoma that is located_in the anal margin.]
sebaceous basal cell carcinoma	DOID_4286
obsolete complications of pregnancy, childbirth and the puerperium	DOID_4285
external ear carcinoma	DOID_4288	[An external ear cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells.]
Polydactyly	HP_0010442	[A congenital anomaly characterized by the presence of supernumerary fingers or toes.]
external ear basal cell carcinoma	DOID_4287
Klippel-Feil syndrome 3	DOID_0080591	[A Klippel-Feil syndrome that has_material_basis_in heterozygous mutation in the GDF3 gene on chromosome 12p13.]
micronodular basal cell carcinoma	DOID_4289	[A basal cell carcinoma characterized by solid tumor nodules.]
Klippel-Feil syndrome 4	DOID_0080592	[A Klippel-Feil syndrome that has_material_basis_in homozygous mutation in the MYO18B gene on chromosome 22q12.]
orofacial cleft 6	DOID_0080593	[An orofacial cleft that has_material_basis_in variation in an enhancer of the IRF6 gene on chromosome 1q32.]
hyper IgE recurrent infection syndrome 2	DOID_0080594	[A hyper IgE syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the DOCK8 gene on chromosome 9p24.]
Klippel-Feil syndrome 2	DOID_0080590	[A Klippel-Feil syndrome that has_material_basis_in homozygous mutation in the MEOX1 gene on chromosome 17q21.]
diaphoresis	SYMP_0019152	[Diaphoresis is a sweat characterized as excessive sweating commonly associated with shock and other medical emergency conditions.]
sweaty	SYMP_0019175	[A skin and integumentary tissue symptom characterized as the excretion of moisture in visible quantities through the opening of the sweat glands.]
hemorrhagic mediastinitis	SYMP_0019154
hematogenous	SYMP_0019156
immunodeficiency-centromeric instability-facial anomalies syndrome 3	DOID_0090010	[An immunodeficiency-centromeric instability-facial anomalies syndrome characterized by autosomal recessive inheritance, recurrent infections in childhood and variable dysmorphic facial features that has_material_basis_in homozygous mutation in the CDCA7 gene on chromosome 2q31.]
immunodeficiency-centromeric instability-facial anomalies syndrome	DOID_0090007	[A syndrome characterized by immunodeficiency, rearrangements in the vicinity of the centromeres of chromosomes 1, 9, and 16 and facial anomalies in most cases.]
eschar	SYMP_0019158	[Eschar is a skin and integumentary tissue symptom characterized as a scab formed especially after a burn.]