Disease Browser
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Parent Node: Nephritis, Hereditary (D009394) | ..Starting node ..Renal Failure, Progressive, with Hypertension (C562889)
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Sister Nodes: | ..Alport syndrome, dominant type (C536586)
| ..Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis (C564570)
| ..Alport syndrome, recessive type (C536587)
| ..ALPORT SYNDROME, X-LINKED (OMIM:301050)
| ..Alport Syndrome-Like Hereditary Nephritis (C562890)
| ..Daentl Towsend Siegel syndrome (C535768)
| ..Deafness nephritis ano rectal malformation (C535996)
| ..Leiomyomatosis, esophageal and vulval, with nephropathy (C537113)
| ..Nephropathy, Progressive, with Deafness (C563713)
| ..Renal Failure, Progressive, with Hypertension (C562889)
| ..Salcedo syndrome (C537228)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 9652 |
Name: | Renal Failure, Progressive, with Hypertension |
Definition: | |
Alternative IDs: | OMIM:161900 |
ParentIDs: | MESH:D009394 |
TreeNumbers: | C12.706.742/C562889 |C12.777.419.570.620/C562889 |C13.351.875.742/C562889 |C13.351.968.419.570.620/C562889 |C16.131.939.742/C562889 |C17.300.200.517/C562889 |
Synonyms: | AORF |Nephritis, Familial, without Deafness or Ocular Defect |Nephropathy, Familial |Renal Failure, Adult-Onset |RFH1 |
Slim Mappings: | Congenital abnormality|Connective tissue disease|Urogenital disease (female)|Urogenital disease (male) |
Reference: |
MedGen: C562889
MeSH: C562889
OMIM: 161900;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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