Showing 1 to 10 of 1811 entries
28 genes associated with this phenotype
Definition: any anomaly in the state or quality of the skin
No IMPC genes are currently associated with this phenotype
Definition: anomaly in the time from the onset of light stimulus to the peak of the b-wave
No IMPC genes are currently associated with this phenotype
Synonym:
reduced striate body size
Definition: reduced size of a large cluster of dopaminergic nerve cells, consisting of the caudate nucleus and the putamen, that controls movement, balance, and walking
No IMPC genes are currently associated with this phenotype
Synonym:
enlarged habenular nucleus
Definition: greater size of the group of nuclei that makes up the small eminence on the dorsomedial surface of the thalamus, just in front of the dorsal commissure on the lateral edge of the habenular trigone
63 genes associated with this phenotype
Synonym:
abnormal blood insulin level
Definition: any anomaly in the blood concentration of the polypeptide hormone, secreted by beta cells of the pancreas, that promotes glucose utilization, protein synthesis, and the formation and storage of neutral lipids
117 genes associated with this phenotype
Synonym:
high mean corpuscular haemoglobin concentration,
high MCHC,
high mean corpuscular hemoglobin concentration,
increased MCHC,
increased mean corpuscular haemoglobin concentration
Definition: greater than the normal Hgb/Hct; the average hemoglobin concentration in a given volume of packed red cells, calculated from the hemoglobin therein and the hematocrit, in erythrocyte indices
No IMPC genes are currently associated with this phenotype
Definition: aberrant differentiation of pulmonary tissues
204 genes associated with this phenotype
Synonym:
lymphocytosis,
increased lymphocyte count
Definition: greater than normal number of the cells involved in adaptive immune reactions of the body in most inflammatory and autoimmune diseases, including B cells, T cells and natural killer cells
No IMPC genes are currently associated with this phenotype
Definition: an increased amount of creatinine in the urine compared to the normal state
1641 genes associated with this phenotype
Synonym:
ophthalmic malformation,
abnormal eyes morphology,
eye: dysmorphology,
eye malformation,
abnormal ocular orb morphology,
eye dysplasia,
ocular dysplasia
Definition: any structural anomaly of the spheroid organ and optic nerve that serves to detect light
Showing 1 to 10 of 1811 entries