Showing 1761 to 1770 of 1817 entries
92 genes associated with this phenotype
Synonym:
optic nerve dysplasia,
abnormal optic II nerve morphology,
abnormal CN-II morphology
Definition: any structural anomaly of the second cranial nerve which is responsible for conveying visual information from the retina to the brain; it extends from the retina to the optic chiasma where part of its fibers become the optic tract and cross to the opposite side and pass to the geniculate bodies
86 genes associated with this phenotype
Definition: anomaly in the size of the elongated structure connected to the posterior surface of the testis that transports, stores, and matures spermatozoa between testis and vas deferens
1 gene associated with this phenotype
Definition: any functional anomaly of the eye as determined through electrophysiological recordings from single cells or summary recordings from multiple cells (e.g. electroretinogram)
No IMPC genes are currently associated with this phenotype
Definition: a greater ear- to -ear distance resulting in the appearance of a wide face and a flattened snout
No IMPC genes are currently associated with this phenotype
Synonym:
fourth ventricle dysplasia,
abnormal ventriculus quartus morphology,
abnormal IVth ventricle morphology,
abnormal rhombencephalic ventricle morphology,
abnormal 4th ventricle morphology,
abnormal ventricle of rhombencephalon morphology
Definition: any structural anomaly of the irregularly shaped cavity in the rhombencephalon, between the medulla oblongata, the pons, and the isthmus in front, and the cerebellum behind; it is continuous with the central canal of the cord below and with the cerebral aqueduct above, and through its lateral and median apertures it communicates with the subarachnoid space
13 genes associated with this phenotype
Synonym:
decreased epididymis size
Definition: decrease in the average size of the elongated structure connected to the posterior surface of the testis that transports, stores, and matures spermatozoa between testis and vas deferens
No IMPC genes are currently associated with this phenotype
Synonym:
abnormal B-1 B-lymphocyte morphology,
abnormal B-1 B lymphocyte morphology,
abnormal B-1 B-cell morphology,
abnormal B1 cell morphology
Definition: any structural anomaly of the subset of B cells found predominantly in the peritoneum, pleural cavities, and spleen, and are enriched for self-reactivity; B-1 B cells are thought to be the primary source of natural IgM immunoglobulin, that is, IgM produced in large quantities without prior antigenic stimulation and generally reactive against various microorganisms, as well as the source of T-independent IgA immunoglobulin in the mucosal areas
No IMPC genes are currently associated with this phenotype
Definition: anomaly in the number of KLRG1-positive CD4-negative NK T cells, a marker associated with activation
No IMPC genes are currently associated with this phenotype
Synonym:
abnormal cerebellar development
Definition: aberrant or incomplete differentiation of the part of the metencephalon that lies dorsal to the pons and medulla behind the brain stem and controls balance for walking and standing, modulates the force and range of movement and is involved in the learning of motor skills
18 genes associated with this phenotype
Definition: any structural anomaly of the mesenchymal outgrowth on the lateral trunk of the embryo that develops into the limbs
Showing 1761 to 1770 of 1817 entries