Hearing Loss Disease Portal


 
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Disease Browser
Parent Node:
expandAbnormalities, Multiple (D000015)
Parent Node:
expandBone Diseases, Developmental (D001848)
Parent Node:
expandCorneal Dystrophies, Hereditary (D003317)
Parent Node:
expandCraniofacial Abnormalities (D019465)
Parent Node:
expandKidney Diseases, Cystic (D052177)
..Starting node
..expandBrachymesomelia renal syndrome (C537096)

       Child Nodes:



 Sister Nodes: 
..expandBaraitser Rodeck Garner syndrome (C537906)
..expandBrachymesomelia renal syndrome (C537096)
..expandCerebrorenodigital Syndrome with Limb Malformations and Triradiate Acetabula (C563731)
..expandCystic Kidney Disease with Ventriculomegaly (C565657)
..expandGlomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria (C563693)
..expandJoubert syndrome 1 (C536293)
..expandJoubert syndrome 2 (C536294)
..expandJoubert syndrome 4 (C536296)
..expandJoubert Syndrome 7 (C566916)
..expandMedullary Sponge Kidney (D007691) Child1
..expandMulticystic Dysplastic Kidney (D021782) Child2
..expandNEPHRONOPHTHISIS 11 (OMIM:613550)
..expandNephronophthisis 2 (C566582)
..expandNephronophthisis 3 (C565780)
..expandNephronophthisis 4 (C564640)
..expandNephronophthisis 7 (C566930)
..expandNephronophthisis, familial juvenile (C537699)
..expandPolycystic Kidney Diseases (D007690) Child21
..expandRenal cysts and diabetes syndrome (C535520)
..expandRENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
..expandSenior Loken Syndrome (C537580)
..expandSenior-Loken Syndrome 3 (C564637)
..expandSenior-Loken syndrome 4 (C537581)
..expandSenior-Loken Syndrome 5 (C563763)
..expandSenior-Loken Syndrome 6 (C565708)
..expandSitus inversus totalis with cystic dysplasia of kidneys and pancreas (C536666)
..expandTsc2 Angiomyolipomas, Renal, Modifier Of (C567682)
..expandUlnar Ray Dysgenesis with Postaxial Polydactyly and Renal Cystic Dysplasia (C565783)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:1430
Name:Brachymesomelia renal syndrome
Definition:
Alternative IDs:
ParentIDs:MESH:D000015|MESH:D001848|MESH:D003317|MESH:D019465|MESH:D052177
TreeNumbers:C05.116.099/C537096 |C05.660.207/C537096 |C11.204.236/C537096 |C11.270.162/C537096 |C12.777.419.403/C537096 |C13.351.968.419.403/C537096 |C16.131.077/C537096 |C16.131.621.207/C537096 |C16.320.290.162/C537096
Synonyms:Brachymesomelia-renal syndrome |Langer Nishino Yamaguchi syndrome
Slim Mappings:Congenital abnormality|Eye disease|Genetic disease (inborn)|Musculoskeletal disease|Urogenital disease (female)|Urogenital disease (male)
Reference: MedGen: C537096
MeSH: C537096
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants