Từ điển y khoa
Thuật ngữ y khoa chuẩn hóa theo MeSH, ICD-11, SNOMED CT.
62,341 terms indexed
Diseases that do not exhibit symptoms.
Infections that do not exhibit symptoms.
RefSeq NM_100845
RefSeq NM_101323
a 3beta-hydroxysteroid dehydrogenase/C-4 decarboxylase
a leucine-rich repeat receptor-like kinase; RefSeq NM_104059
RefSeq NM_104861
RefSeq NM_105862
Gene ID: 843861
RefSeq NP_178414
RefSeq NM_129976
a pentatricopeptide repeat protein; RefSeq NM_130052
a pentapeptide repeat protein; RefSeq NM_130056
Gene ID: 820002
a cellulose-binding protein; RefSeq NM_111682
RefSeq NM_113223
RefSeq NM_113308
RefSeq NM_114392
RefSeq NM_114706
RefSeq NM_115627.4
RefSeq NM_116352
RefSeq NM_116710
RefSeq NM_117534
MDA1 - MTERF DEFECTIVE IN Arabidopsis1; RefSeq NM_117541
RefSeq NM_118751
RefSeq NM_119518
a B-box protein that promotes photomorphogenesis downstream of both brassinosteroid and light signaling pathways; RefSeq NM_120067.7
Gene ID: 831157
RefSeq NM_121955
RefSeq NM_124172
RefSeq NM_116733
RefSeq NM_100059
RefSeq NM_129656
RefSeq NM_136045
RefSeq NM_179203
A genus of ADENOVIRIDAE that comprises viruses of several species of MAMMALS and BIRDS. The type species is Ovine adenovirus D.
Impairment of the ability to perform smoothly coordinated voluntary movements. This condition may affect the limbs, trunk, eyes, pharynx, larynx, and other structures. Ataxia may result from impaired sensory or motor function. Sensory ataxia may result from posterior column injury or PERIPHERAL NERVE DISEASES. Motor ataxia may be associated with CEREBELLAR DISEASES; CEREBRAL CORTEX diseases; THALAMIC DISEASES; BASAL GANGLIA DISEASES; injury to the RED NUCLEUS; and other conditions.
An autosomal recessive inherited disorder characterized by choreoathetosis beginning in childhood, progressive CEREBELLAR ATAXIA; TELANGIECTASIS of CONJUNCTIVA and SKIN; DYSARTHRIA; B- and T-cell immunodeficiency, and RADIOSENSITIVITY to IONIZING RADIATION. Affected individuals are prone to recurrent sinobronchopulmonary infections, lymphoreticular neoplasms, and other malignancies. Serum ALPHA-FETOPROTEINS are usually elevated. (Menkes, Textbook of Child Neurology, 5th ed, p688) The gene for this disorder (ATM) encodes a cell cycle checkpoint protein kinase and has been mapped to chromosome 11 (11q22-q23).
mutation in MRE11A