771
|
|
|
Collagen type V alpha 3 chain |
- |
|
772
|
|
|
Carbohydrate sulfotransferase 11 |
C4ST, C4ST-1, C4ST1, HSA269537, OCBMD |
|
773
|
|
|
Calcyon neuron specific vesicular protein |
DRD1IP, NSG3 |
|
774
|
|
|
Contactin 3 |
BIG-1, PANG, PCS |
|
775
|
|
|
COP9 signalosome subunit 7A |
CSN7, CSN7A, SGN7a |
|
776
|
|
|
Cell adhesion associated, oncogene regulated |
CDO, CDON1, HPE11, Ihog, ORCAM |
Agenesis of corpus callosum, Alobar holoprosencephaly, Ambiguous genitalia, Asthma, Choanal atresia, Congenital coloboma of iris, Congenital hypoplasia of penis, Cryptorchidism, Cyclocephaly, Developmental delay, Diabetes insipidus, Duodenal atresia, Dwarfism, Fused incisors, Gastrointestinal stromal tumor, Hemangioma, Holoprosencephaly, Hypoglycemia, Hypothyroidism, Kidney failure, Lobar holoprosencephaly, Mental retardation, Microcephaly, Microform holoprosencephaly, Midline interhemispheric variant of holoprosencephaly, Panhypopituitarism, Physiologic amenorrhea, Pituitary stalk interruption syndrome, Polysplenia, Proptosis, Renal agenesis, Scoliosis, Semilobar holoprosencephaly, Septo-optic dysplasia, Septopreoptic holoprosencephaly, Strabismus, Synophrys, Tetralogy of fallotView all (23 more) |
777
|
|
|
Coenzyme Q6, monooxygenase |
CGI-10, CGI10, COQ10D6 |
|
778
|
|
|
CutC copper transporter |
CGI-32 |
|
779
|
|
|
Crystallin lambda 1 |
GDH, HEL30, gul3DH, lambda-CRY |
|
780
|
|
|
Coenzyme Q4 |
CGI-92, COQ10D7, SPAX10 |
|