Entry Search - 210370 608614 - OMIM
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Search: '210370 608614 (Search in: MIM number)'
Results: 2 entries.

2:
# 210370. BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY; BCD
Cytogenetic location: 4q35.1-q35.2
Matching terms: 210370
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
4q35.1-q35.2 Bietti crystalline corneoretinal dystrophy 210370 AR 3 CYP4V2 608614
ICD+
SNOMEDCT: 312927001
ORPHA: 41751
DO: 0050664
Search: 210370 608614 (Search in: MIM number)
Results: 2 entries.

1:
* 608614. CYTOCHROME P450, FAMILY 4, SUBFAMILY V, POLYPEPTIDE 2; CYP4V2
Cytogenetic location: 4q35.1-q35.2, Genomic coordinates (GRCh38): 4:186,191,567-186,213,463
Matching terms: 608614

2:
# 210370. BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY; BCD
Cytogenetic location: 4q35.1-q35.2
Matching terms: 210370