Entry Search - 236700 604896 - OMIM
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Search: '236700 604896 (Search in: MIM number)'
Results: 2 entries.

1:
* 604896. MKKS CENTROSOMAL SHUTTLING PROTEIN; MKKS
Cytogenetic location: 20p12.2, Genomic coordinates (GRCh38): 20:10,401,009-10,434,222
Matching terms: 604896
► Gene-Phenotype Relationships  ► ICD+  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
20p12.2 Bardet-Biedl syndrome 6 605231 AR 3
McKusick-Kaufman syndrome 236700 AR 3
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ICD+
SNOMEDCT: 702407009
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2:
# 236700. MCKUSICK-KAUFMAN SYNDROME; MKKS
Cytogenetic location: 20p12.2
Matching terms: 236700
► Phenotype-Gene Relationships  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
20p12.2 McKusick-Kaufman syndrome 236700 AR 3 MKKS 604896
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ICD+
SNOMEDCT: 702407009
ORPHA: 2473
DO: 0111255
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Search: 236700 604896 (Search in: MIM number)
Results: 2 entries.

1:
* 604896. MKKS CENTROSOMAL SHUTTLING PROTEIN; MKKS
Cytogenetic location: 20p12.2, Genomic coordinates (GRCh38): 20:10,401,009-10,434,222
Matching terms: 604896

2:
# 236700. MCKUSICK-KAUFMAN SYNDROME; MKKS
Cytogenetic location: 20p12.2
Matching terms: 236700


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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