Terminology Service < Semantic Lookup Platform

All terms in HP

Label	Id	Description
Abnormality of the corticospinal tract	HP_0002492	[Abnormality of the corticospinal tract, which is the chief element of the pyramidal system (the principle motor tract) and is the only direct connection between the cerebrum and the spinal cord.]
Morphological abnormality of the pyramidal tract	HP_0002062	[Any structural abnormality of the pyramidal tract, whose chief element, the corticospinal tract, is the only direct connection between the brain and the spinal cord. In addition to the corticospinal tract, the pyramidal system includes the corticobulbar, corticomesencephalic, and corticopontine tracts.]
Impaired vibratory sensation	HP_0002495	[A decrease in the ability to perceive vibration. Clinically, this is usually tested with a tuning fork which vibrates at 128 Hz and is applied to bony prominences such as the malleoli at the ankles or the metacarpal-phalangeal joints. There is a slow decay of vibration from the tuning fork. The degree of vibratory sense loss can be crudely estimated by counting the number of seconds that the examiner can perceive the vibration longer than the patient.]
Sensory impairment	HP_0003474	[An abnormality of the primary sensation that is mediated by peripheral nerves (pain, temperature, touch, vibration, joint position). The word hypoesthesia (or hypesthesia) refers to a reduction in cutaneous sensation to a specific type of testing.]
Abnormal rapid eye movement sleep	HP_0002494	[Abnormality of REM sleep. Phases of REM sleep are characterized by desynchronized EEG patterns, increases in heart rate and blood pressure, sympathetic activation, and a profound loss of muscle tonus except for the eye and middle-ear muscles. There are then phases of rapid eye movements.]
Sleep-wake cycle disturbance	HP_0006979	[Any abnormal alteration of an individual's circadian rhythm that affects the timing of sleeping and being awake.]
Microgastria	HP_0100841	[A developmental anomaly wtih a small tubular or saccular midline stomach.]
muscle organ development	GO_0007517	[The process whose specific outcome is the progression of the muscle over time, from its formation to the mature structure. The muscle is an organ consisting of a tissue made up of various elongated cells that are specialized to contract and thus to produce movement and mechanical work.]
muscle structure development	GO_0061061	[The progression of a muscle structure over time, from its formation to its mature state. Muscle structures are contractile cells, tissues or organs that are found in multicellular organisms.]
kdr (zebrafish)	ZDB-GENE-041001-112	[A protein coding gene kdr in zebrafish.]
Danio rerio	NCBITaxon_7955
obsolete Glioblastoma	HP_0100843
Spasticity of facial muscles	HP_0002491	[Spasticity of one or more muscles innervated by the facial nerve.]
Abnormality of facial musculature	HP_0000301	[An anomaly of a muscle that is innervated by the facial nerve (the seventh cranial nerve).]
Septo-optic dysplasia	HP_0100842	[Underdevelopment of the optic nerve and absence of the septum pellucidum.]
Optic nerve hypoplasia	HP_0000609	[Underdevelopment of the optic nerve.]
Absent septum pellucidum	HP_0001331	[Absence of the septum pellucidum.]
Increased CSF lactate	HP_0002490	[Increased concentration of lactate in the cerebrospinal fluid.]
Abnormal CSF lactate level	HP_0030085	[Abnormal concentration of lactate in the cerebrospinal fluid.]
Anaphylactic shock	HP_0100845	[An acute hypersensitivity reaction due to exposure to a previously encountered antigen.]