Terminology Service < Semantic Lookup Platform

All individuals in MESHD

Label	Id	Description
Jaw Cysts	D007570	[Saccular lesions lined with epithelium and contained within pathologically formed cavities in the jaw; also nonepithelial cysts (pseudocysts) as they apply to the jaw, e.g., traumatic or solitary cyst, static bone cavity, and aneurysmal bone cyst. True jaw cysts are classified as odontogenic or nonodontogenic.]
Jaw Diseases	D007571	[Diseases involving the JAW.]
Jaw Fractures	D007572	[Fractures of the upper or lower jaw.]
Jaw Neoplasms	D007573	[Cancers or tumors of the MAXILLA or MANDIBLE unspecified. For neoplasms of the maxilla, MAXILLARY NEOPLASMS is available and of the mandible, MANDIBULAR NEOPLASMS is available.]
Jaw, Edentulous	D007575	[The total absence of teeth from either the mandible or the maxilla, but not both. Total absence of teeth from both is MOUTH, EDENTULOUS. Partial absence of teeth in either is JAW, EDENTULOUS, PARTIALLY.]
Jaw, Edentulous, Partially	D007576	[Absence of teeth from a portion of the mandible and/or maxilla.]
Jejunal Diseases	D007579	[Pathological development in the JEJUNUM region of the SMALL INTESTINE.]
Jejunal Neoplasms	D007580	[Tumors or cancer in the JEJUNUM region of the small intestine (INTESTINE, SMALL).]
Jervell-Lange Nielsen Syndrome	D029593	[A form of long QT syndrome that is associated with congenital deafness. It is characterized by abnormal cardioelectrophysiology involving the VOLTAGE-GATED POTASSIUM CHANNEL. It results from mutation of KCNQ1 gene (Subtype 1 or JLN1) or the KCNE1 gene (Subtype 2 or JLN2).]
Jet Lag Syndrome	D020179	[A chronobiologic disorder resulting from rapid travel across a number of time zones, characterized by insomnia or hypersomnolence, fatigue, behavioral symptoms, headaches, and gastrointestinal disturbances. (From Cooper, Sleep, 1994, pp593-8)]
Job Syndrome	D007589	[Primary immunodeficiency syndrome characterized by recurrent infections and hyperimmunoglobulinemia E. Most cases are sporadic. Of the rare familial forms, the dominantly inherited subtype has additional connective tissue, dental and skeletal involvement that the recessive type does not share.]
Joint Deformities, Acquired	D016916	[Deformities acquired after birth as the result of injury or disease. The joint deformity is often associated with rheumatoid arthritis and leprosy.]
Joint Diseases	D007592	[Diseases involving the JOINTS.]
Joint Dislocations	D004204	[Partial or incomplete displacement of an articulation., Displacement of bones from their normal positions at a joint.]
Joint Instability	D007593	[Lack of stability of a joint or joint prosthesis.]
Joint Loose Bodies	D007594	[Fibrous, bony, cartilaginous and osteocartilaginous fragments in a synovial joint. Major causes are osteochondritis dissecans, synovial chondromatosis, osteophytes, fractured articular surfaces and damaged menisci.]
Kallmann Syndrome	D017436	[A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait., Type 2 is an autosomal dominant form with loss-of-function mutations of gene Kal2 which encodes fibroblast growth-factor receptor-1 (FGFR1 PROTEIN)., Type 1 is the X-linked form with mutations of gene Kal1 which encodes anosmin-1 protein that plays a key role in the migration of GNRH-containing neurons and olfactory nerves to the HYPOTHALAMUS.]
Kaposi Varicelliform Eruption	D007617	[A disseminated vesicular-pustular eruption caused by the herpes simplex virus (HERPESVIRUS HOMINIS), the VACCINIA VIRUS, or Varicella zoster (HERPESVIRUS 3, HUMAN). It is usually superimposed on a preexisting, inactive or active, atopic dermatitis (DERMATITIS, ATOPIC).]
Karoshi Death	D065907	[Sudden death from overwork, most often as a result of acute CARDIOVASCULAR STROKE.]
Kartagener Syndrome	D007619	[An autosomal recessive disorder characterized by a triad of DEXTROCARDIA; INFERTILITY; and SINUSITIS. The syndrome is caused by mutations of DYNEIN genes encoding motility proteins which are components of sperm tails, and CILIA in the respiratory and the reproductive tracts.]