All terms in DOID

Label Id Description
obsolete Streptomyces somaliensis infectious disease DOID_0050003
obsolete Actinomadura pelletieri infectious disease DOID_0050002
lung mixed small cell and squamous cell carcinoma DOID_7081
metal cation CHEBI_25213
inorganic cation CHEBI_36915
monoatomic cation CHEBI_23906
obsolete recurrent adult primary liver cancer DOID_7084
obsolete recurrent adult primary hepatoma DOID_7083
malignant melanocytic peripheral nerve sheath tumor of mediastinum DOID_7077
obsolete malignant mediastinal peripheral nerve sheath tumor DOID_7078
obsolete atypical vulvar nevus DOID_7075
breast lipid-rich carcinoma DOID_7076 [A lipid-rich carcinoma characterized by the presence of cytoplasmic neutral lipids in the vast majority of the malignant cells.]
adult cystic teratoma DOID_7079 [A cystic teratoma that is present in an adult.]
cystic teratoma DOID_2660 [A benign teratoma that is characterized by the presence of cysts or cystic spaces.]
seminal vesicle acute gonorrhea DOID_0050004 [A gonococcal seminal vesiculitis that is characterized by back pain, perineal pain, pain with ejaculation, hematospermia and voiding symptoms resulting from inflammation located_in the seminal vesicles caused by Neisseria gonorrhoeae infection.]
obsolete cutaneous strongyloidiasis DOID_0050007 [A strongyloidiasis that involves parasitic infection by the filariform larvae of Strongyloides stercoralis, which penetrate the human skin causing urticarial rashes in the buttocks and waist areas.]
obsolete intestinal strongyloidiasis DOID_0050009 [A strongyloidiasis that involves infection of intestine with Strongyloides stercoralis, which results in abdominal pain, diarrhea, ileus, massive gastrointestinal bleeding, severe malabsorption, and peritonitis.]
metatropic dysplasia DOID_0111514 [A spondyloepimetaphyseal dysplasia characterized by short limbs with limitation and enlargement of joints, usually severe and progressive kyphoscoliosis, severe platyspondyly, and severe metaphyseal enlargement that has_material_basis_in heterozygous mutation in the TRPV4 gene on chromosome 12q24.11.]
quinolines CHEBI_26513
autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2 DOID_0111515 [A chronic progressive external ophthalmoplegia characterized by adult onset of progressive external ophthalmoplegia, exercise intolerance, muscle weakness, and signs and symptoms of spinocerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the RNASEH1 gene on chromosome 2p25.3.]