Showing 1771 to 1780 of 1817 entries
No IMPC genes are currently associated with this phenotype
Synonym:
abnormal B lymphocyte number,
abnormal B-cell number
Definition: deviation from the normal count of cells that are formed in the bone marrow, migrate to the peripheral lymphatic system, and mature into plasma cells or memory cells; these cells are involved in humoral immunity
11 genes associated with this phenotype
Definition: any structural anomaly of the portion of the small intestine that extends from the duodenum to the ileum
1 gene associated with this phenotype
Synonym:
reduced pre-pro B cell number
Definition: reduced number of pro-B cells that are CD45R/B220-positive, CD43-positive, HSA-low, BP-1-negative and Ly6c-negative; this cell type is also described as being lin-negative, AA4-positive, Kit-positive, IL7Ra-positive and CD45R-positive
No IMPC genes are currently associated with this phenotype
Synonym:
facial nerve dysplasia,
abnormal CN-VII morphology
Definition: any structural anomaly of the sensory and motor nerve that supplies the muscles of facial expression and the expression and taste at the anterior two-thirds of the tongue; principal branches are the superficial opthalmic, buccal, palatine and hyomandibular
248 genes associated with this phenotype
Synonym:
abnormal ocular blood vessel morphology,
abnormal eye blood vessel morphology,
abnormal ocular vasculature morphology
Definition: any anomaly of the structure or arrangement of blood vessels supplying the eye
3 genes associated with this phenotype
Synonym:
mechanical nociception abnormalities
Definition: abnormal capability to sense pain elicited by mechanical stimulation
170 genes associated with this phenotype
Synonym:
vertebral anomaly,
vertebra dysplasia
Definition: any structural anomaly of the bony segments of the spinal column
No IMPC genes are currently associated with this phenotype
Synonym:
abnormal cerebellar gyri morphology,
abnormal cerebellar folia morphology
Definition: any structural anomaly of the ten gyri of the cerebellar cortex
3 genes associated with this phenotype
Definition: increase in the number of dendritic cells expressing low levels of CD11b which usually express CD8, depend on Irf8 and Batf3 for their development and are responsible for cross-presentation
48 genes associated with this phenotype
Synonym:
polydactylia,
polydactylism,
hyperdactyly
Definition: greater than the normal complement of digits on one or more autopods
Showing 1771 to 1780 of 1817 entries