Entry Search - 221200 609681 - OMIM
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Search: '221200 609681 (Search in: MIM number)'
Results: 2 entries.

1:
* 609681. SLIT- AND NTRK-LIKE FAMILY, MEMBER 6; SLITRK6
Cytogenetic location: 13q31.1, Genomic coordinates (GRCh38): 13:85,792,790-85,799,419
Matching terms: 609681
► Gene-Phenotype Relationships  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
13q31.1 Deafness and myopia 221200 AR 3
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2:
# 221200. DEAFNESS AND MYOPIA; DFNMYP
Cytogenetic location: 13q31.1
Matching terms: 221200
► Phenotype-Gene Relationships  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
13q31.1 Deafness and myopia 221200 AR 3 SLITRK6 609681
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ICD+
ORPHA: 363396
DO: 0111628
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Search: 221200 609681 (Search in: MIM number)
Results: 2 entries.

1:
* 609681. SLIT- AND NTRK-LIKE FAMILY, MEMBER 6; SLITRK6
Cytogenetic location: 13q31.1, Genomic coordinates (GRCh38): 13:85,792,790-85,799,419
Matching terms: 609681

2:
# 221200. DEAFNESS AND MYOPIA; DFNMYP
Cytogenetic location: 13q31.1
Matching terms: 221200


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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