Entry Search - 120110 156500 - OMIM
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Search: '120110 156500 (Search in: MIM number)'
Results: 2 entries.

1:
* 120110. COLLAGEN, TYPE X, ALPHA-1; COL10A1
Cytogenetic location: 6q22.1, Genomic coordinates (GRCh38): 6:116,118,909-116,217,144
Matching terms: 120110
► Gene-Phenotype Relationships  ► ICD+  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
6q22.1 Metaphyseal chondrodysplasia, Schmid type 156500 AD 3
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ICD+
SNOMEDCT: 29248006
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2:
# 156500. METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS
Cytogenetic location: 6q22.1
Matching terms: 156500
► Phenotype-Gene Relationships  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
6q22.1 Metaphyseal chondrodysplasia, Schmid type 156500 AD 3 COL10A1 120110
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ICD+
SNOMEDCT: 29248006
ORPHA: 174
DO: 0080021
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Search: 120110 156500 (Search in: MIM number)
Results: 2 entries.

1:
* 120110. COLLAGEN, TYPE X, ALPHA-1; COL10A1
Cytogenetic location: 6q22.1, Genomic coordinates (GRCh38): 6:116,118,909-116,217,144
Matching terms: 120110

2:
# 156500. METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS
Cytogenetic location: 6q22.1
Matching terms: 156500


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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