Terminology Service < Semantic Lookup Platform

All terms in MESHD

Label	Id	Description
Skull Neoplasms	D012888	[Neoplasms of the bony part of the skull.]
Respiratory Tract Neoplasms	D012142	[New abnormal growth of tissue in the RESPIRATORY SYSTEM.]
Glucose Metabolism Disorders	D044882	[Pathological conditions in which the BLOOD GLUCOSE cannot be maintained within the normal range, such as in HYPOGLYCEMIA and HYPERGLYCEMIA. Etiology of these disorders varies. Plasma glucose concentration is critical to survival for it is the predominant fuel for the CENTRAL NERVOUS SYSTEM.]
Hypolipoproteinemias	D007009	[Conditions with abnormally low levels of LIPOPROTEINS in the blood. This may involve any of the lipoprotein subclasses, including ALPHA-LIPOPROTEINS (high-density lipoproteins); BETA-LIPOPROTEINS (low-density lipoproteins); and PREBETA-LIPOPROTEINS (very-low-density lipoproteins)., A condition with abnormally low levels of PREBETA-LIPOPROTEINS in the blood.]
Dyslipidemias	D050171	[Abnormalities in the serum levels of LIPIDS, including overproduction or deficiency. Abnormal serum lipid profiles may include high total CHOLESTEROL, high TRIGLYCERIDES, low HIGH DENSITY LIPOPROTEIN CHOLESTEROL, and elevated LOW DENSITY LIPOPROTEIN CHOLESTEROL.]
Lipid Metabolism, Inborn Errors	D008052	[Errors in the metabolism of LIPIDS resulting from inborn genetic MUTATIONS that are heritable.]
Hypokalemia	D007008	[Abnormally low potassium concentration in the blood. It may result from potassium loss by renal secretion or by the gastrointestinal route, as by vomiting or diarrhea. It may be manifested clinically by neuromuscular disorders ranging from weakness to paralysis, by electrocardiographic abnormalities (depression of the T wave and elevation of the U wave), by renal disease, and by gastrointestinal disorders. (Dorland, 27th ed)]
Mandibular Neoplasms	D008339	[Tumors or cancer of the MANDIBLE.]
Hypohidrosis	D007007	[Abnormally diminished or absent perspiration. Both generalized and segmented (reduced or absent sweating in circumscribed locations) forms of the disease are usually associated with other underlying conditions.]
Sweat Gland Diseases	D013543	[Diseases of the SWEAT GLANDS.]
Mandibular Injuries	D008338	[Injuries to the lower jaw bone.]
Nose Deformities, Acquired	D009667	[Abnormalities of the nose acquired after birth from injury or disease.]
Hypogonadism	D007006	[Condition resulting from deficient gonadal functions, such as GAMETOGENESIS and the production of GONADAL STEROID HORMONES. It is characterized by delay in GROWTH, germ cell maturation, and development of secondary sex characteristics. Hypogonadism can be due to a deficiency of GONADOTROPINS (hypogonadotropic hypogonadism) or due to primary gonadal failure (hypergonadotropic hypogonadism).]
Gonadal Disorders	D006058	[Pathological processes of the OVARIES or the TESTES.]
Mandibular Fractures	D008337	[Fractures of the lower jaw.]
Synkinesis	D046608	[An involuntary movement accompanying a volitional movement. It often refers to facial movements that accompany FACIAL PARALYSIS.]
Dyskinesias	D020820	[Abnormal involuntary movements which primarily affect the extremities, trunk, or jaw that occur as a manifestation of an underlying disease process. Conditions which feature recurrent or persistent episodes of dyskinesia as a primary manifestation of disease may be referred to as dyskinesia syndromes (see MOVEMENT DISORDERS). Dyskinesias are also a relatively common manifestation of BASAL GANGLIA DISEASES.]
Gonadal Dysgenesis, 46,XX	D023961	[The 46,XX gonadal dysgenesis may be sporadic or familial. Familial XX gonadal dysgenesis is transmitted as an autosomal recessive trait and its locus was mapped to chromosome 2. Mutation in the gene for the FSH receptor (RECEPTORS, FSH) was detected. Sporadic XX gonadal dysgenesis is heterogeneous and has been associated with trisomy-13 and trisomy-18. These phenotypic females are characterized by a normal stature, sexual infantilism, bilateral streak gonads, amenorrhea, elevated plasma LUTEINIZING HORMONE and FSH concentration.]
Gonadal Dysgenesis	D006059	[A number of syndromes with defective gonadal developments such as streak GONADS and dysgenetic testes or ovaries. The spectrum of gonadal and sexual abnormalities is reflected in their varied sex chromosome (SEX CHROMOSOMES) constitution as shown by the karyotypes of 45,X monosomy (TURNER SYNDROME); 46,XX (GONADAL DYSGENESIS, 46XX); 46,XY (GONADAL DYSGENESIS, 46,XY); and sex chromosome MOSAICISM; (GONADAL DYSGENESIS, MIXED). Their phenotypes range from female, through ambiguous, to male. This concept includes gonadal agenesis., The complete failure of gonadal development.]
46, XX Disorders of Sex Development	D058489	[Congenital conditions in individuals with a female karyotype, in which the development of the gonadal or anatomical sex is atypical.]