Entry Search - 223360 609312 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '223360 609312 (Search in: MIM number)'
Results: 2 entries.

1:
* 609312. DOPAMINE BETA-HYDROXYLASE, PLASMA; DBH
Cytogenetic location: 9q34.2, Genomic coordinates (GRCh38): 9:133,636,363-133,659,329
Matching terms: 609312
► Gene-Phenotype Relationships  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
9q34.2 Orthostatic hypotension 1, due to DBH deficiency 223360 AR 3
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2:
# 223360. ORTHOSTATIC HYPOTENSION 1; ORTHYP1
Cytogenetic location: 9q34.2
Matching terms: 223360
► Phenotype-Gene Relationships  ► Phenotypic Series  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
9q34.2 Orthostatic hypotension 1, due to DBH deficiency 223360 AR 3 DBH 609312
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Orthostatic hypotension - PS223360 - 2 Entries
Location Phenotype Inheritance Phenotype
mapping key 		Phenotype
MIM number 		Gene/Locus Gene/Locus
MIM number
9q34.2 Orthostatic hypotension 1, due to DBH deficiency AR 3 223360 DBH 609312
17q23.3 Orthostatic hypotension 2 AR 3 618182 CYB561 600019
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ICD+
SNOMEDCT: 237923004
ORPHA: 230
DO: 0090145
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Search: 223360 609312 (Search in: MIM number)
Results: 2 entries.

1:
* 609312. DOPAMINE BETA-HYDROXYLASE, PLASMA; DBH
Cytogenetic location: 9q34.2, Genomic coordinates (GRCh38): 9:133,636,363-133,659,329
Matching terms: 609312

2:
# 223360. ORTHOSTATIC HYPOTENSION 1; ORTHYP1
Cytogenetic location: 9q34.2
Matching terms: 223360


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OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 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® 1966-2024 Johns Hopkins University.
Printed: April 23, 2024