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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/163800
http://purl.bioontology.org/ontology/OMIM/163800
|
|---|---|
| Preferred Name | SICK SINUS SYNDROME 2 |
| Synonyms |
ATRIAL FIBRILLATION WITH BRADYARRHYTHMIA
SINUS BRADYCARDIA SYNDROME, FAMILIAL, AUTOSOMAL DOMINANT
SINUS NODE DISEASE, FAMILIAL, AUTOSOMAL DOMINANT
SICK SINUS SYNDROME 2 WITH OR WITHOUT CARDIAC NONCOMPACTION AND/OR ASCENDING AORTA DILATION
SSS2
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel | ATRIAL FIBRILLATION WITH BRADYARRHYTHMIA
SINUS BRADYCARDIA SYNDROME, FAMILIAL, AUTOSOMAL DOMINANT
SINUS NODE DISEASE, FAMILIAL, AUTOSOMAL DOMINANT
SICK SINUS SYNDROME 2 WITH OR WITHOUT CARDIAC NONCOMPACTION AND/OR ASCENDING AORTA DILATION
SSS2
|
|---|---|
| prefLabel | SICK SINUS SYNDROME 2
|
| Gene Symbol |
HCN4
SSS2
EIG18
BRGDA8
|
| Scope Statement | Caused by mutation in the hyperpolarization-activated cyclic nucleotide-gated potassium channel 4 gene (HCN4, 605206.0001) [MOLECULAR BASIS]
Onset in utero or at birth [MISCELLANEOUS]
|
| type | |
| Has manifestation |
See more
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|
| tui | T047
|
| Gene Locus | 15q24-q25
|
| MIMTYPEMEANING | Phenotype description, molecular basis known.
|
| notation | 163800
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C1834144
|
| OMIM Entry Type | 3
|
| OMIM MimType Value | pound
|
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |