Entry Search - 162100 604061 - OMIM
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Search: '162100 604061 (Search in: MIM number)'
Results: 2 entries.

1:
* 604061. SEPTIN 9; SEPTIN9
Cytogenetic location: 17q25.3, Genomic coordinates (GRCh38): 17:77,281,499-77,500,596
Matching terms: 604061
► Gene-Phenotype Relationships  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
17q25.3 Amyotrophy, hereditary neuralgic 162100 AD 3
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2:
# 162100. AMYOTROPHY, HEREDITARY NEURALGIC; HNA
Cytogenetic location: 17q25.3
Matching terms: 162100
► Phenotype-Gene Relationships  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
17q25.3 Amyotrophy, hereditary neuralgic 162100 AD 3 SEPT9 604061
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ICD+
ORPHA: 2901
DO: 10383
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Search: 162100 604061 (Search in: MIM number)
Results: 2 entries.

1:
* 604061. SEPTIN 9; SEPTIN9
Cytogenetic location: 17q25.3, Genomic coordinates (GRCh38): 17:77,281,499-77,500,596
Matching terms: 604061

2:
# 162100. AMYOTROPHY, HEREDITARY NEURALGIC; HNA
Cytogenetic location: 17q25.3
Matching terms: 162100


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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 14, 2025