All terms in HP

Label Id Description
Syntelencephaly HP_0025670 [Syntelencephaly is a rare malformation that consists of an abnormal midline connection of the cerebral hemispheres in the posterior frontal and parietal regions, with interhemispheric separation of the basal forebrain, anterior frontal lobes, and occipital regions.]
cell hair GO_0070451 [A long, thin cell projection that contains F-actin and tubulin, with microtubules centrally located and F-actin peripherally located.]
prolactin secretion GO_0070459 [The regulated release of prolactin, a peptide hormone that stimulates lactation, from secretory granules in the anterior pituitary.]
Abnormality of glycosaminoglycan metabolism HP_0004371 [Abnormality of glycosaminoglycan metabolism.]
Moderate to late preterm birth HP_0025664 [Birth at 32 to 36 completed weeks of gestation.]
Extremely preterm birth HP_0025665 [Birth before 28 completed weeks of gestation (up to and including 27 weeks and 6 days of gestation).]
lysinium(1+) CHEBI_32564 [An alpha-amino-acid cation that is the conjugate acid of lysine, having two cationic amino groups and an anionic carboxy group.]
lysinium(2+) CHEBI_32565 [An alpha-amino-acid cation obtained by protonation of both amino groups of lysine.]
Reduced fetal femur/foot length ratio HP_0025663 [This ratio relates the length of the fetal femur to that of the fetal foot. The ratio is approximately 1 throughout the age range of 14 to 40 weeks of gestation. A substantial reduction in the raio can help differentiate fetuses that have dysplastic limb reduction from those whose limbs are short because of constitutional factors or IUGR. It can reduce the problem of an unknown gestational age and help to distinguish between fetal skeletal dysplasia and intrauterine growth retardation caused by other factors.]
lysinate CHEBI_32563 [An alpha-amino-acid anion that is the conjugate base of lysine, arising from deprotonation of the carboxy group.]
Very preterm birth HP_0025666 [Birth before 32 completed weeks of gestation (28 up to but not including 32 weeks).]
Chiari type II malformation HP_0025660 [A type of Chiari malformation that consists of brainstem herniation and a towering cerebellum in addition to the herniated cerebellar tonsils and vermis due to an open distal spinal dysraphism/myelomeningocele.]
Chiari type III malformation HP_0025661 [A type of Chiari malformation that involves herniation of the hindbrain (cerebellum with or without the brainstem) into a low occipital or high cervical meningoencephalocele.]
Decreased urine output HP_0011037 [A decreased rate of urine production.]
Fibrin casts HP_0025697 [A type of airway casts that consist of plasma components and inflammatory cells.]
Airway casts HP_0025696 [A replicate of airways from accumulated and condensed mucous and cellular material. These semisolid occlusions take the shape of the airway within they are formed, leading to obstruction of the tracheobronchial tree with consecutive respiratory insufficiency. Based on their principal composition, one can differentiate fibrin casts and mucin casts. Plastic bronchitis is the name of the condition characterized by the formation of airway casts.]
Mucin casts HP_0025698 [A type of airway casts that consist of impacted mucus.]
histidinium(1+) CHEBI_32531
Mucus plug HP_0025695 [Mucus that is abnormally thick in consistency (ie, inspissated) and plugs the airway is known as a mucus plug. Mucus plugs consist of mucins and cells and can partially or completely obstruct one or more airways and cause serious consequences, including atelectasis and recurrent infection.]
histidinium(2+) CHEBI_32532