All terms in HP

Label Id Description
Progressive sensorineural hearing impairment HP_0000408 [A progressive form of sensorineural hearing impairment.]
Progressive hearing impairment HP_0001730 [A progressive form of hearing impairment.]
collection of basal ganglia UBERON_0010011 [Subcortical masses of gray matter in the forebrain and midbrain that are richly interconnected and so viewed as a functional system. The nuclei usually included are the caudate nucleus (caudoputamen in rodents), putamen, globus pallidus, substantia nigra (pars compacta and pars reticulata) and the subthalamic nucleus. Some also include the nucleus accumbens and ventral pallidum.]
negative regulation of protein O-linked glycosylation GO_1904099 [Any process that stops, prevents or reduces the frequency, rate or extent of protein O-linked glycosylation.]
negative regulation of glycoprotein biosynthetic process GO_0010561 [Any process that decreases the rate, frequency, or extent of the chemical reactions and pathways resulting in the formation of a glycoprotein, a protein that contains covalently bound glycose (i.e. monosaccharide) residues; the glycose occurs most commonly as oligosaccharide or fairly small polysaccharide but occasionally as monosaccharide.]
regulation of protein O-linked glycosylation GO_1904098 [Any process that modulates the frequency, rate or extent of protein O-linked glycosylation.]
Recurrent otitis media HP_0000403 [Increased susceptibility to otitis media, as manifested by recurrent episodes of otitis media.]
Otitis media HP_0000388 [Inflammation or infection of the middle ear.]
regulation of glycoprotein biosynthetic process GO_0010559 [Any process that modulates the rate, frequency, or extent of the chemical reactions and pathways resulting in the formation of a glycoprotein, a protein that contains covalently bound glycose (i.e. monosaccharide) residues; the glycose occurs most commonly as oligosaccharide or fairly small polysaccharide but occasionally as monosaccharide.]
Functional abnormality of the middle ear HP_0011452 [An abnormality of the function of the middle ear.]
Abnormality of the outer ear HP_0000356 [An abnormality of the external ear.]
Cupped ear HP_0000378 [Laterally protruding ear that lacks antihelical folding (including absence of inferior and superior crura).]
S-adenosyl-L-homocysteine zwitterion CHEBI_57856 [Zwitterionic form of S-adenosyl-L-homocysteine arising from migration of a proton from the carboxy group to the alpha-amino group; major species at pH 7.3.]
Abnormal cochlea morphology HP_0000375 [An abnormality of the cochlea.]
Abnormal inner ear morphology HP_0011390 [A structural anomaly of the internal part of the ear.]
Incomplete partition of the cochlea type II HP_0000376 [With incomplete partition II, the cochlea consists of 1.5 turns; the apical and middle cochlea turns are undifferentiated and form a cystic apex. The vestibule is normal while the vestibular aqueduct is always enlarged. Developmental arrest occurs at the seventh week of gestation.]
Incomplete partition of the cochlea HP_0011373 [Incomplete formation of the cochlear partition. The scala vestibuli and scala tympani separated by the cochlear partition, except in the apical turn where the two scalae are in continuity via the helicotrema.]
Abnormal ear morphology HP_0031703 [Any structural anomaly of the ear.]
Acute otitis media HP_0000371 [Acute otitis media is a short and generally painful infection of the middle ear.]
Abnormal mannosylation of N-linked protein glycosylation HP_0012355 [An anomaly of the addition of mannose to N-linked glycans.]