All terms in HP

Label Id Description
leucinate CHEBI_32627 [An alpha-amino-acid anion that is the conjugate base of leucine, arising from deprotonation of the carboxy group.]
branched-chain amino-acid anion CHEBI_63471 [A branched-chain amino acid whose alpha-carboxylic acid group is ionized.]
leucinium CHEBI_32628 [An alpha-amino-acid cation that is the conjugate acid of leucine, arising from protonation of the amino group.]
Birth length greater than 97th percentile HP_0003517
obsolete Abnormality of cartilage morphology HP_0410007
Abnormality of the somatic nervous system HP_0410009 [Any abnormality of the part of the peripheral nervous system associated with sensation and skeletal muscle voluntary control of body movements.]
Luteinizing hormone CHEBI_81568
obsolete Cleft maxillary alveolus HP_0410003
obsolete Cleft secondary palate HP_0410004
Abnormal vomer morphology HP_0410000 [An abnormality of the vomer.]
5-methyltetrahydrofolate CHEBI_20612 [A group of heterocyclic compounds based on the 5-methyl-5,6,7,8-tetrahydropteroic acid skeleton conjugated with one or more L-glutamic acid or L-glutamate units.]
Decreased glucosephosphate isomerase level HP_0003568 [A decreased level of glucose-6-phosphate isomerase.]
Folate-dependent fragile site at Xq28 HP_0003564 [The presence of a folate sensitive fragile site at chromosome Xq28.]
Decreased LDL cholesterol concentration HP_0003563 [An decreased concentration of low-density lipoprotein cholesterol in the blood.]
Increased serum prostaglandin E2 HP_0003566 [An increased concentration of prostaglandin E2 in the blood.]
Abnormal circulating prostaglandin circulation HP_0011023 [Any deviation from the normal concentration of a prostaglandin in the blood circulation.]
obsolete Abnormal radial ray morphology HP_0410049
Elevated erythrocyte sedimentation rate HP_0003565 [An increased erythrocyte sedimentation rate (ESR). The ESR is a test that measures the distance that erythrocytes have fallen after one hour in a vertical column of anticoagulated blood under the influence of gravity. The ESR is a nonspecific finding. An elevation may indicate inflammation or may be caused by any condition that elevates fibrinogen.]
Muscular dystrophy HP_0003560 [The term dystrophy means abnormal growth. However, muscular dystrophy is used to describe primary myopathies with a genetic basis and a progressive course characterized by progressive skeletal muscle weakness and wasting, defects in muscle proteins, and histological features of muscle fiber degeneration (necrosis) and regeneration. If possible, it is preferred to use other HPO terms to describe the precise phenotypic abnormalities.]
Abnormal neural tube morphology HP_0410043 [Any structural anomaly of the hollow epithelial tube found on the dorsal side of the vertebrate embryo that develops into the central nervous system (i.e. brain and spinal cord).]