Terminology Service < Semantic Lookup Platform

All terms in HP

Label	Id	Description
gland	UBERON_0002530	[an organ that functions as a secretory or excretory organ]
respiratory system	UBERON_0001004	[Functional system which consists of structures involved in respiration.]
Deficit in phonologic short-term memory	HP_0002549
Parkinsonism with favorable response to dopaminergic medication	HP_0002548	[Parkinsonism is a clinical syndrome that is a feature of a number of different diseases, including Parkinson disease itself, other neurodegenerative diseases such as progressive supranuclear palsy, and as a side-effect of some neuroleptic medications. Some but not all individuals with Parkinsonism show responsiveness to dopaminergic medication defined as a substantial reduction of amelioration of the component signs of Parkinsonism (including mainly tremor, bradykinesia, rigidity, and postural instability) upon administration of dopaminergic medication.]
Parkinsonism	HP_0001300	[Characteristic neurologic anomaly resulting form degeneration of dopamine-generating cells in the substantia nigra, a region of the midbrain, characterized clinically by shaking, rigidity, slowness of movement and difficulty with walking and gait.]
gland of nasal mucosa	UBERON_0012278	[The nasal glands are the seromucous glands in the respiratory region of the nasal mucous membrane. The three major types of nasal glands are anterior serous glands, seromucous glands, and Bowman glands.]
nasal cavity mucosa	UBERON_0001826	[The mucous membrane that lines the nasal cavity[MP].]
Abnormal arachnoid mater morphology	HP_0100700	[An abnormality of the Arachnoid mater.]
Abnormal meningeal morphology	HP_0010651	[An abnormality of the Meninges, including any abnormality of the Dura mater, the Arachnoid mater, and the Pia mater.]
Arachnoid cyst	HP_0100702	[An extra-parenchymal and intra-arachnoidal collection of fluid with a composition similar to that of cerebrospinal fluid.]
Abnormal pia mater	HP_0100701	[An abnormality of the pia mater.]
Cerebral visual impairment	HP_0100704	[A form of loss of vision caused by damage to the visual cortex rather than a defect in the eye.]
Visual impairment	HP_0000505	[Visual impairment (or vision impairment) is vision loss (of a person) to such a degree as to qualify as an additional support need through a significant limitation of visual capability resulting from either disease, trauma, or congenital or degenerative conditions that cannot be corrected by conventional means, such as refractive correction, medication, or surgery.]
Tongue thrusting	HP_0100703
Stereotypy	HP_0000733	[A stereotypy is a repetitive, simple movement that can be voluntarily suppressed. Stereotypies are typically simple back-and-forth movements such as waving of flapping the hands or arms, and they do not involve complex sequences or movement fragments. Movement is often but not always rhythmic and may involve fingers, wrists, or more proximal portions of the upper extremity. The lower extremity is not typically involved. Stereotypies are more commonly bilateral than unilateral.]
Abnormality of the oligodendroglia	HP_0100706	[One of the three types of glia cells that, with the nerve cells, compose the central nervous system and are characterized by sheetlike processes that wrap around individual axons to form the myelin sheath of nerve fibers.]
Abnormality of the glial cells	HP_0100705	[An abnormality of the glia cell.]
Abnormality of the microglia	HP_0100708	[An abnormality of the microglial cells. They are also known as brain-resident macrophages or hortega cells.]
Abnormality of the immune system	HP_0002715	[An abnormality of the immune system.]
Abnormality of the astrocytes	HP_0100707	[An abnormality of astrocytes.]