All terms in DOID

Label Id Description
sexual health disorder DOID_0060043 [A disease of mental health that involves the impairment in normal sexual functioning.]
abdominal aortic aneurysm DOID_7693 [An aortic aneurysm that is located_in the abdominal aorta.]
pineal parenchymal tumor of intermediate differentiation DOID_5030
pineoblastoma DOID_1664 [A pineal gland neoplasm located_in the brain.]
bladder urachal adenocarcinoma DOID_7694
obsolete renal cell carcinoma with constitutional chromosome 3 translocations DOID_6361
adult pineal parenchymal tumor DOID_5031
pancreatic ACTH hormone producing tumor DOID_7697
acral lentiginous melanoma DOID_6367 [A skin melanoma that is characterized by slow growth of a small pigmented spot on the skin with a clearly defined edge, surrounded by normal-appearing skin and occurs on occurs on non hair-bairing surfaces including hands and feet, subungual sites, and fingers or toes.]
non-functioning pancreatic endocrine tumor DOID_7698
lung hilum cancer DOID_7696
congenital myopathy 2C DOID_0081340 [A congenital myopathy that is characterized by severe congenital weakness usually resulting in death from respiratory failure in the first year or so of life and that has_material_basis_in heterozygous mutation in the ACTA1 gene on chromosome 1q42. Heterozygous mutation in the ACTA1 gene can also cause autosomal dominant typical congenital myopathy-2A (CMYP2A). Biallelic mutation in the ACTA1 gene causes autosomal recessive severe infantile congenital myopathy-2B (CMYP2B).]
congenital myopathy 5 DOID_0081341 [A congenital myopathy that is characterized by the onset of muscle weakness in infancy manifest as neonatal hypotonia, delayed motor development, and often distal contractures and that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding titin (TTN) on chromosome 2q31.]
myoblastoma DOID_5039
congenital myopathy 8 DOID_0081342 [A congenital myopathy that is characterized by hypotonia and delayed motor development apparent from infancy or childhood, resulting in difficulties walking or loss of ambulation within the first few decades and that has_material_basis_in heterozygous mutation in the ACTN2 gene on chromosome 1q43. Heterozygous mutation in the ACTN2 gene can also cause distal myopathy-6 (MPD6), which shows later onset and is less severe.]
Abnormality of vision HP_0000504
Visual impairment HP_0000505
extraventricular neurocytoma DOID_0081314 [A cerebral ventricle cancer that is characterized by the presence of neoplastic uniform, round cells with neuronal differentiation, that arises from the brain parenchyma. Unlike central neurocytoma, it does not involve the lateral ventricles.]
obsolete asthenopia DOID_10141
central nervous system tumor with BCOR internal tandem duplication DOID_0081315 [A central nervous system embryonal tumor that is characterized by the presence of uniform oval or spindle-shaped cells with round or oval nuclei, pseudorosette formation, and heterozygous internal tandem duplication in exon 15 of the BCOR gene.]