Disease #03285

Official abbreviation CSNB-1C
Name blindness, night, stationary, congenital, type 1C (CSNB-1C)
OMIM ID 613216
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 6
Phenotype entries for this disease 6
Associated with 1 gene TRPM1
Associated tissues -
Disease features -
Remarks -


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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00033591 - - - M no India Indian - 0 - - CSNB-1C - TRPM1 TRPM1 2 1 Soumittra Nagasamy
00033592 - - - F yes India Indian - 0 - - CSNB-1C - TRPM1 TRPM1 1 1 Soumittra Nagasamy
00033593 - - - M yes India Indian - 0 - - CSNB-1C - TRPM1 TRPM1 2 1 Soumittra Nagasamy
00033594 - - - M yes India Indian - 0 - - CSNB-1C - TRPM1 TRPM1 2 1 Soumittra Nagasamy
00033595 - - - F no India Indian - 0 - - CSNB-1C - TRPM1 TRPM1 2 1 Soumittra Nagasamy
00033596 - - - F yes India Indian - 0 - - CSNB-1C - TRPM1 TRPM1 1 1 Soumittra Nagasamy
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