Mutant rhodopsin or beta subunit of retinal rod cGMP phosphodiesterase
Symptom Information:
|
Symptom ID:
|
OMIM : No Id available
|
|
Synonyms:
|
|
|
Quality:
|
|
|
Cross references:
|
| OMIM: "Mutant rhodopsin or beta subunit of retinal rod cGMP phosphodiesterase" [OMIM:Mutant rhodopsin or beta subunit of retinal rod cGMP phosphodiesterase] |
|
|
Is a (Direct Parents):
|
|
|
Is a (Whole tree):
|
HPO:
MedDRA:
|
|
Database Frequency:
|
1 / 7739
|
|
Resource:
|
|
All diseases associated with this symptom:
|
NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2
|
(OMIM:163500)
|