All terms in HP

Label Id Description
Herpes simplex encephalitis HP_0012302 [Infection of the brain parenchyma with herpes simplex virus, resulting in inflammation of the brain parenchyma with neurologic dysfunction.]
Viral encephalitis HP_0033993 [An inflammation of brain parenchyma due to infection with a virus. Viral encephalitis can occur as a rare complication of common infections (eg, herpes virus infections) or can occur as a characteristic presentation of rare viruses (eg, rabies virus infection). Encephalitis may be the only neurologic manifestation of infection, or may occur in association with meningitis, myelitis, radiculitis, or neuritis. Viral encephalitis is associated with neurological dysfunction.]
regulation of bleb assembly GO_1904170 [Any process that modulates the frequency, rate or extent of bleb assembly.]
regulation of plasma membrane bounded cell projection assembly GO_0120032 [Any process that modulates the rate, frequency, or extent of plasma membrane bounded cell projection assembly.]
Type II transferrin isoform profile HP_0012301 [Abnormal transferrin isoform profile consistent with a type II congenital disorder of glycosylation.]
Abnormal isoelectric focusing of serum transferrin HP_0003160 [Glycosylated transferrin concentrations can be measured in serum as a marker of N-linked glycosylation fidelity. In the traditional nomenclature for congenital disorders of glycosylation, absence of entire glycans was designated type I, and loss of one or more monosaccharides as type II. These terms are retained for historical reasons but for new annotations the precise glycosylation defect should be recorded.]
positive regulation of bleb assembly GO_1904172 [Any process that activates or increases the frequency, rate or extent of bleb assembly.]
positive regulation of plasma membrane bounded cell projection assembly GO_0120034 [Any process that activates or increases the frequency, rate or extent of plasma membrane bounded cell projection assembly.]
negative regulation of bleb assembly GO_1904171 [Any process that stops, prevents or reduces the frequency, rate or extent of bleb assembly.]
negative regulation of plasma membrane bounded cell projection assembly GO_0120033 [Any process that stops, prevents or reduces the frequency, rate or extent of plasma membrane bounded cell projection assembly.]
positive regulation of monoatomic ion transmembrane transport GO_0034767 [Any process that activates or increases the frequency, rate or extent of the directed movement of ions from one side of a membrane to the other.]
positive regulation of monoatomic ion transport GO_0043270 [Any process that activates or increases the frequency, rate or extent of the directed movement of charged atoms or small charged molecules into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.]
negative regulation of response to nutrient levels GO_0032108 [Any process that stops, prevents, or reduces the frequency, rate or extent of a response to nutrient levels.]
regulation of response to nutrient levels GO_0032107 [Any process that modulates the frequency, rate or extent of a response to nutrient levels.]
Abnormal maxilla morphology HP_0000326 [An abnormality of the Maxilla (upper jaw bone).]
Abnormal jaw morphology HP_0030791 [A structural anomaly of the jaw, the bony structure of the mouth that consists of the mandible and the maxilla.]
positive regulation of response to nutrient levels GO_0032109 [Any process that activates or increases the frequency, rate or extent of a response to nutrient levels.]
Hypoplasia of the maxilla HP_0000327 [Abnormally small dimension of the Maxilla. Usually creating a malocclusion or malalignment between the upper and lower teeth or resulting in a deficient amount of projection of the base of the nose and lower midface region.]
ulcer MPATH_579 [Loss of epithelium and the basement membrane (full thickness). Cf Erosion.]
cell and tissue damage MPATH_1 [The sum of morphological and functional disturbances induced by cell and tissue damage, either from intrinsic gene dysfunction or as a result of external factors.]