Entry Search - 605268 606438 - OMIM
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Search: '605268 606438 (Search in: MIM number)'
Results: 2 entries.

1:
# 606438. HUNTINGTON DISEASE-LIKE 2; HDL2
Cytogenetic location: 16q24.2
Matching terms: 606438
► Phenotype-Gene Relationships  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
16q24.2 Huntington disease-like 2 606438 AD 3 JPH3 605268
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ICD+
SNOMEDCT: 721228006
ORPHA: 98934
DO: 0090104
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2:
* 605268. JUNCTOPHILIN 3; JPH3
Cytogenetic location: 16q24.2, Genomic coordinates (GRCh38): 16:87,601,835-87,698,156
Matching terms: 605268
► Gene-Phenotype Relationships  ► ICD+  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
16q24.2 Huntington disease-like 2 606438 AD 3
▲ Close
ICD+
SNOMEDCT: 721228006
▲ Close
Search: 605268 606438 (Search in: MIM number)
Results: 2 entries.

1:
# 606438. HUNTINGTON DISEASE-LIKE 2; HDL2
Cytogenetic location: 16q24.2
Matching terms: 606438

2:
* 605268. JUNCTOPHILIN 3; JPH3
Cytogenetic location: 16q24.2, Genomic coordinates (GRCh38): 16:87,601,835-87,698,156
Matching terms: 605268


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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