Showing 31 to 40 of 1817 entries
417 genes associated with this phenotype
Synonym:
growth/weight/body size abnormality: embryonic
Definition: limited or accelerated growth or development apparent during the embryonic period (sensu Mus: up to E14, or the completion of organogenesis)
13 genes associated with this phenotype
Synonym:
microalbuminuria,
increased microalbumin excretion
Definition: greater than the normal amount of microalbumin in the urine
24 genes associated with this phenotype
Synonym:
humoural immune response dysfunction,
humoral immune response dysfunction,
antibody-mediated immune response abnormalities,
abnormal humoural immune response
Definition: any functional anomaly of the aspect of immunity that is mediated by secreted antibodies produced in the cells of the B lymphocyte lineage (B cell) and the accessory processes that accompany it, including Th2 activation and cytokine production, germinal center formation and isotype switching, affinity maturation and memory cell generation; it also refers to the effector functions of antibody, which include pathogen and toxin neutralization, classical complement activation, and opsonin promotion of phagocytosis and pathogen elimination
No IMPC genes are currently associated with this phenotype
Definition: increase in material stiffness (N/mm) during elastic deformation in the femur
42 genes associated with this phenotype
Definition: congenital fissure of the tissues normally uniting to form the palate
19 genes associated with this phenotype
Synonym:
pupil dilation,
enlarged pupils,
large pupils,
large pupil,
dilated pupil,
enlarged pupil,
dilated pupils,
increased pupil size
Definition: increased diameter of one or both central circular aperture of the iris through which light rays enter the eye
No IMPC genes are currently associated with this phenotype
Synonym:
abnormal mature natural killer cell morphology,
abnormal lymphokine activated killer cell morphology
Definition: any structural anomaly of NK cells expressing the maturation marker CD11b
786 genes associated with this phenotype
Synonym:
abnormal glands morphology,
glands: dysmorphology,
glandular dysplasia
Definition: any structural anomaly of an organ that functions as a secretory or excretory organ
17 genes associated with this phenotype
Synonym:
decreased PR interval,
reduced PR interval
Definition: decrease in the length of time between the beginning of atrial depolarization and the beginning of ventricular depolarization, measured by the interval from the beginning of the P wave to the beginning of the QRS complex
1313 genes associated with this phenotype
Synonym:
cardiovascular dysplasia,
cardiovascular system dysplasia,
heart/cardiovascular system: dysmorphology
Definition: any structural anomaly of the heart or vascular tissue
Showing 31 to 40 of 1817 entries