Results for "osteoarthritis with mild chondrodysplasia": 34 genes

Name

USH2A Gene

Usher syndrome 2A (autosomal recessive, mild)

This gene encodes a protein that contains laminin EGF motifs, a pentaxin domain, and many fibronectin type III motifs. The protein is found in the basement membrane, and may be important in development and homeostasis of the inner ear and retina. Mutations within this gene have been associated with Usher syndrome type IIa and retinitis pigmentosa. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]

OS4 Gene

Osteoarthritis, generalized, without dysplasia, susceptibility to

OS6 Gene

Osteoarthritis susceptibility 6

OA10 Gene

Osteoarthritis QTL 10

OA30 Gene

Osteoarthritis QTL 29

OSTEAR3_H Gene

Osteoarthritis QTL 3

OA26 Gene

Osteoarthritis QTL 26

OA25 Gene

Osteoarthritis QTL 25

OA27 Gene

Osteoarthritis QTL 27

OA24 Gene

Osteoarthritis QTL 24

OA22 Gene

Osteoarthritis QTL 22

OA23 Gene

Osteoarthritis QTL 23

OA20 Gene

Osteoarthritis QTL 20

OA21 Gene

Osteoarthritis QTL 21

OA28 Gene

Osteoarthritis QTL 28

OA29 Gene

Osteoarthritis QTL 29

CCAL1 Gene

chondrocalcinosis 1 (calcium pyrophosphate-deposition disease, early onset osteoarthritis)

OA7 Gene

Osteoarthritis QTL 7

OA6 Gene

Osteoarthritis QTL 6

OA5 Gene

Osteoarthritis QTL 5

OA4 Gene

Osteoarthritis QTL 4

OA2 Gene

Osteoarthritis QTL 2

OA1 Gene

Osteoarthritis QTL 1

OA9 Gene

Osteoarthritis QTL 9

OA8 Gene

Osteoarthritis QTL 8

OA19 Gene

Osteoarthritis QTL 19

OA18 Gene

Osteoarthritis QTL 18

OA13 Gene

Osteoarthritis QTL 13

OA12 Gene

Osteoarthritis QTL 12

OA11 Gene

Osteoarthritis QTL 11

OA17 Gene

Osteoarthritis QTL 17

OA16 Gene

Osteoarthritis QTL 16

OA15 Gene

Osteoarthritis QTL 15

OA14 Gene

Osteoarthritis QTL 14