Showing 1661 to 1670 of 1817 entries
thin hippocampus stratum radiatum
No IMPC genes are currently associated with this phenotype
Synonym:
Definition: decrease in the width of the layer located immediately above the pyramidal cell layer in CA2 and CA1 and superficial to the stratum lucidum in CA3
abnormal heart shape
14 genes associated with this phenotype
Synonym:
heart shape abnormalities
Definition: any anomaly in the characteristic surface outline or contour of the heart
abnormal ear position
1 gene associated with this phenotype
Synonym:
abnormal position of pinna,
abnormal pinnae position,
abnormal pinna position,
abnormal ear distance/ position
Definition: anomaly in the space between or the placement of the outer ears
abnormal craniofacial morphology
384 genes associated with this phenotype
Synonym:
craniofacial dysplasia
Definition: any structural anomaly of the face or head affecting appearance
increased susceptibility to bacterial infection
No IMPC genes are currently associated with this phenotype
Synonym:
decreased resistance to bacterial infection
Definition: greater likelihood that an organism will develop ill effects from a bacterial infection or from components of or toxins produced by bacteria
increased brain size
13 genes associated with this phenotype
Synonym:
macroencephaly,
larger brain size,
megalencephaly,
enlarged brain,
megaloencephaly,
macrencephaly
Definition: larger than the normal physical proportions of the brain
abnormal ventral commissure morphology
No IMPC genes are currently associated with this phenotype
Synonym:
Definition: any structural anomaly of the fiber tracts that connect the ventral region of the two cerebral hemispheres and span the longitudinal fissure, including the anterior and the habenular commissures
abnormal nervous system physiology
443 genes associated with this phenotype
Synonym:
Definition: any functional anomaly of the extensive, intricate network of electochemical structures in the body that is comprised of the brain, spinal cord, nerves, ganglia and parts of the receptor organs that receive and interpret stimuli and transmit impulses to effector organs to control body functions
decreased IgG1 level
2 genes associated with this phenotype
Synonym:
reduced IgG1 level
Definition: less than normal immunoglobulin class G1 level
abnormal stomach morphology
61 genes associated with this phenotype
Synonym:
gastric dysplasia,
abnormal gastric morphology,
stomach dysplasia
Definition: any structural anomaly of the hollow, sac-like structure of the digestive canal between the esophagus and the small intestine that functions to emulsify food
Showing 1661 to 1670 of 1817 entries