Terminology Service < Semantic Lookup Platform

All individuals in MESHD

Label	Id	Description
Halitosis	D006209	[An offensive, foul breath odor resulting from a variety of causes such as poor oral hygiene, dental or oral infections, or the ingestion of certain foods.]
Hallermann's Syndrome	D006210	[An oculomandibulofacial syndrome principally characterized by dyscephaly (usually brachycephaly), parrot nose, mandibular hypoplasia, proportionate nanism, hypotrichosis, bilateral congenital cataracts, and microphthalmia. (Dorland, 27th ed)]
Hallucinations	D006212	[Subjectively experienced sensations in the absence of an appropriate stimulus, but which are regarded by the individual as real. They may be of organic origin or associated with MENTAL DISORDERS.]
Hallux Limitus	D020857	[A bony proliferation and articular degeneration of the first METATARSOPHALANGEAL JOINT that is characterized by pain and a progressive decrease in the dorsiflexion range of motion.]
Hallux Rigidus	D020859	[A condition caused by degenerative arthritis (see OSTEOARTHRITIS) of the METATARSOPHALANGEAL JOINT of the great toe and characterized by pain and limited dorsiflexion, but relatively unrestricted plantar flexion.]
Hallux Valgus	D006215	[Lateral displacement of the great toe (HALLUX), producing deformity of the first METATARSOPHALANGEAL JOINT with callous, bursa, or bunion formation over the bony prominence.]
Hallux Varus	D050488	[Displacement of the great toe (HALLUX) towards the midline or away from the other TOES. It can be congenital or acquired., Angulation of the first metatarsal bone towards the midline. This is associated with angulation of the phalanges of the same toe away from the midline (HALLUX VALGUS).]
Hamartoma	D006222	[A focal malformation resembling a neoplasm, composed of an overgrowth of mature cells and tissues that normally occur in the affected area.]
Hamartoma Syndrome, Multiple	D006223	[A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Facial trichilemmomas and papillomatous papules of the oral mucosa are the most characteristic lesions. Individuals with this syndrome have a high risk of BREAST CANCER; THYROID CANCER; and ENDOMETRIAL CANCER. This syndrome is associated with mutations in the gene for PTEN PHOSPHATASE.]
Hammer Toe Syndrome	D037801	[A condition characterized by a series of interrelated digital symptoms and joint changes of the lesser digits and METATARSOPHALANGEAL JOINTS of the FOOT. The syndrome can include some or all of the following conditions: hammer toe, claw toe, mallet toe, overlapping fifth toe, curly toe, EXOSTOSIS; HYPEROSTOSIS; interdigital heloma, or contracted toe.]
Hand Deformities	D006226	[Alterations or deviations from normal shape or size which result in a disfigurement of the hand.]
Hand Deformities, Acquired	D006227	[Deformities of the hand, or a part of the hand, acquired after birth as the result of injury or disease.]
Hand Deformities, Congenital	D006228	[Alterations or deviations from normal shape or size which result in a disfigurement of the hand occurring at or before birth.]
Hand Dermatoses	D006229	[Skin diseases involving the HANDS.]
Hand Injuries	D006230	[General or unspecified injuries to the hand.]
Hand, Foot and Mouth Disease	D006232	[A mild, highly infectious viral disease of children, characterized by vesicular lesions in the mouth and on the hands and feet. It is caused by coxsackieviruses A.]
Hand-Arm Vibration Syndrome	D053421	[An occupational disorder resulting from prolonged exposure to vibration, affecting the fingers, hands, and forearms. It occurs in workers who regularly use vibrating tools such as jackhammers, power chain saws, riveters, etc. Symptoms include episodic finger blanching, NUMBNESS, tingling, and loss of nerve sensitivity.]
Hand-Foot Syndrome	D060831	[Chemotherapy-induced dermal side effects that are associated with the use of various CYTOSTATIC AGENTS. Symptoms range from mild ERYTHEMA and/or PARESTHESIA to severe ulcerative dermatitis with debilitating pain involving typically palmoplantar and intertriginous areas. These cutaneous manifestations are sometimes accompanied by nail anomalies.]
Hantavirus Infections	D018778	[Infections with viruses of the genus HANTAVIRUS. This is associated with at least four clinical syndromes: HEMORRHAGIC FEVER WITH RENAL SYNDROME caused by viruses of the Hantaan group; a milder form of HFRS caused by SEOUL VIRUS; nephropathia epidemica caused by PUUMALA VIRUS; and HANTAVIRUS PULMONARY SYNDROME caused by SIN NOMBRE VIRUS.]
Hantavirus Pulmonary Syndrome	D018804	[Acute respiratory illness in humans caused by the SIN NOMBRE VIRUS whose primary rodent reservoir is the deer mouse Peromyscus maniculatus. First identified in the southwestern United States, this syndrome is characterized most commonly by fever, myalgias, headache, cough, and rapid respiratory failure.]