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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/161900
http://purl.bioontology.org/ontology/OMIM/161900
|
|---|---|
| Preferred Name | RENAL FAILURE, PROGRESSIVE, WITH HYPERTENSION |
| Synonyms |
NEPHROPATHY, FAMILIAL
RENAL FAILURE, ADULT-ONSET
RFH1
AORF
NEPHRITIS, FAMILIAL, WITHOUT DEAFNESS OR OCULAR DEFECT
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
NEPHROPATHY, FAMILIAL
RENAL FAILURE, ADULT-ONSET
RFH1
AORF
NEPHRITIS, FAMILIAL, WITHOUT DEAFNESS OR OCULAR DEFECT
|
|---|---|
| prefLabel | RENAL FAILURE, PROGRESSIVE, WITH HYPERTENSION
|
| Gene Symbol |
AORF
RFH1
|
| Scope Statement | Onset in young adulthood or adulthood [MISCELLANEOUS]
One family has been reported (last curated December 2012) [MISCELLANEOUS]
Hypertension is presenting sign [MISCELLANEOUS]
Progressive disorder [MISCELLANEOUS]
|
| type | |
| Has manifestation |
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|
| tui | T047
|
| Gene Locus | 1q21
|
| MIMTYPEMEANING | Mendelian phenotype or locus, molecular basis unknown.
|
| notation | 161900
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C0403443
|
| OMIM Entry Type | 5
|
| OMIM MimType Value | perc
|
| Delete | Subject | Author | Type | Created |
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| No notes to display |