All terms in HP

Label Id Description
Deficit in phonologic short-term memory HP_0002549 [Impaired ability to repeat non-word sounds. The test for nonword repetition involves the repetition of nonsensical words of increasing length and complexity and is regarded as a measure of phonological (speech sound) processing and short-term memory]
Short term memory impairment HP_0033687 [A deficit in the retention of pieces of information (memory chunks) for a relatively short time (usually up to 30 seconds).]
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 from 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.]
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 [Pressing forward of the tongue in the mouth, a retained motoric habit from infantile swallowing patterns]
Stereotypic movements of face and head HP_5200017 [Abnormal movements of face and head.]
Abnormal oligodendroglia morphology 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.]
Abnormal glial cell morphology HP_0100705 [An abnormality of the glia cell.]
Abnormal nervous system morphology HP_0012639 [A structural anomaly of the nervous system.]
Abnormal microglia morphology HP_0100708 [An abnormality of the microglial cells. They are also known as brain-resident macrophages or Hortega cells.]
Abnormal astrocyte morphology HP_0100707 [An abnormality of astrocytes.]
Reduction of oligodendroglia HP_0100709
Abnormal thoracic spine morphology HP_0100711 [An abnormality of the thoracic vertebral column.]