Entry Search - 125255 610048 - OMIM
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Search: '125255 610048 (Search in: MIM number)'
Results: 2 entries.

1:
* 125255. DECORIN; DCN
Cytogenetic location: 12q21.33, Genomic coordinates (GRCh38): 12:91,140,484-91,182,817
Matching terms: 125255
► Gene-Phenotype Relationships  ► ICD+  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
12q21.33 Corneal dystrophy, congenital stromal 610048 AD 3
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ICD+
SNOMEDCT: 702359002
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2:
# 610048. CORNEAL DYSTROPHY, CONGENITAL STROMAL; CSCD
Cytogenetic location: 12q21.33
Matching terms: 610048
► Phenotype-Gene Relationships  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
12q21.33 Corneal dystrophy, congenital stromal 610048 AD 3 DCN 125255
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ICD+
SNOMEDCT: 702359002
ORPHA: 101068
DO: 0060445
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Search: 125255 610048 (Search in: MIM number)
Results: 2 entries.

1:
* 125255. DECORIN; DCN
Cytogenetic location: 12q21.33, Genomic coordinates (GRCh38): 12:91,140,484-91,182,817
Matching terms: 125255

2:
# 610048. CORNEAL DYSTROPHY, CONGENITAL STROMAL; CSCD
Cytogenetic location: 12q21.33
Matching terms: 610048


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OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2025 Johns Hopkins University.

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2025 Johns Hopkins University.
Printed: March 5, 2025