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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/613677
http://purl.bioontology.org/ontology/OMIM/613677
|
|---|---|
| Preferred Name | HYPERALDOSTERONISM, FAMILIAL, TYPE III |
| Synonyms |
FH III
HALD3
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
FH III
HALD3
|
|---|---|
| prefLabel | HYPERALDOSTERONISM, FAMILIAL, TYPE III
|
| Gene Symbol |
KATP1
KCNJ5
LQT13
GIRK4
|
| Scope Statement | Onset of symptoms in first decade of life [MISCELLANEOUS]
Caused by mutation in the member-5 subfamily-J inwardly rectifying potassium channel gene (KCNJ5, 600734.0002) [MOLECULAR BASIS]
Patients with medication-resistant hypertension require bilateral adrenalectomy [MISCELLANEOUS]
|
| type | |
| Has manifestation |
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|
| tui | T047
|
| Gene Locus | 11q24
|
| MIMTYPEMEANING | Phenotype description, molecular basis known.
|
| notation | 613677
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C3838758
|
| OMIM Entry Type | 3
|
| OMIM MimType Value | pound
|
| Delete | Subject | Author | Type | Created |
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| No notes to display |