Showing 1801 to 1810 of 1817 entries
abnormal thoracic cage morphology
110 genes associated with this phenotype
Synonym:
abnormal thoracic basket morphology,
abnormal rib cage morphology,
abnormal ribcage morphology
Definition: any structural anomaly of the bony and cartilaginous structure enclosing the thoracic cavity, consisting of the thoracic vertebrae, ribs, costal cartilages, and sternum
decreased dendritic epidermal T cell number
1 gene associated with this phenotype
Synonym:
Definition: reduction in the number of T cells with dendritic appearance residing in the skin epidermis, usually expressing a canonical gamma-delta T cell receptor and is involved in the regulation of wound healing
increased piriform cortex size
No IMPC genes are currently associated with this phenotype
Synonym:
enlarged piriform cortex
Definition: increased size of the subdivision of the laminated olfactory cortex with only three main layers that receive monosynaptic input from the olfactory bulb via the lateral olfactory tract
abnormal enzyme/coenzyme level
1104 genes associated with this phenotype
Synonym:
Definition: altered level of any enzyme or their cofactors, that act as catalysts to induce chemical changes in other substances
abnormal exploration in a new environment
497 genes associated with this phenotype
Synonym:
Definition: anomaly in the amount of time spent investigating new location
decreased b-wave implicit time
No IMPC genes are currently associated with this phenotype
Synonym:
faster b-wave implicit time
Definition: decrease in the time from the onset of light stimulus to the peak of the b-wave
abnormal defecation amount
5 genes associated with this phenotype
Synonym:
abnormal defaecation amount
Definition: anomaly in the amount of discharge of feces from the body compared to the control
abnormal heart rate
241 genes associated with this phenotype
Synonym:
Definition: greater than or fewer than average resting heart beats per minute, usually measured by the number of times the heart ventricles contract per unit of time, usually per minute
increased mean corpuscular hemoglobin
215 genes associated with this phenotype
Synonym:
hyperchromia,
increased mean corpuscular haemoglobin,
increased MCH,
high mean corpuscular hemoglobin,
high mean corpuscular haemoglobin,
high MCH
Definition: greater than the average levels of hemoglobin contained in an erythrocyte
abnormal skin condition
30 genes associated with this phenotype
Synonym:
Definition: any anomaly in the state or quality of the skin
Showing 1801 to 1810 of 1817 entries