Entry Search - 118661 143200 - OMIM
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Search: '118661 143200 (Search in: MIM number)'
Results: 2 entries.

2:
# 143200. WAGNER VITREORETINOPATHY; WGVRP
Cytogenetic location: 5q14.2-q14.3
Matching terms: 143200
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
5q14.2-q14.3 Wagner syndrome 1 143200 AD 3 VCAN 118661
ICD+
SNOMEDCT: 232064001
ORPHA: 898
Search: 118661 143200 (Search in: MIM number)
Results: 2 entries.

1:
* 118661. VERSICAN; VCAN
Cytogenetic location: 5q14.2-q14.3, Genomic coordinates (GRCh38): 5:83,471,744-83,582,302
Matching terms: 118661

2:
# 143200. WAGNER VITREORETINOPATHY; WGVRP
Cytogenetic location: 5q14.2-q14.3
Matching terms: 143200