Entry Search - 603309 617360 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '603309 617360 (Search in: MIM number)'
Results: 2 entries.

1:
* 603309. CYCLIN-DEPENDENT KINASE 13; CDK13
Cytogenetic location: 7p14.1, Genomic coordinates (GRCh38): 7:39,950,256-40,099,580
Matching terms: 603309
► Gene-Phenotype Relationships  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
7p14.1 Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder 617360 AD 3
▲ Close

2:
# 617360. CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD
Cytogenetic location: 7p14.1
Matching terms: 617360
► Phenotype-Gene Relationships  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
7p14.1 Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder 617360 AD 3 CDK13 603309
▲ Close
ICD+
ORPHA: 646278
DO: 0112247
▲ Close
Search: 603309 617360 (Search in: MIM number)
Results: 2 entries.

1:
* 603309. CYCLIN-DEPENDENT KINASE 13; CDK13
Cytogenetic location: 7p14.1, Genomic coordinates (GRCh38): 7:39,950,256-40,099,580
Matching terms: 603309

2:
# 617360. CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD
Cytogenetic location: 7p14.1
Matching terms: 617360


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.

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