Send us a Message

Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   


RGD uses the Human Disease Ontology (DO, for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:X-linked nephrolithiasis type I
go back to main search page
Accession:DOID:0111798 term browser browse the term
Definition:A renal tubular transport disease characterized by proximal renal tubular reabsorptive failure, hypercalciuria, nephrolithiasis, and renal insufficiency with absence of rickets that has_material_basis_in hemizygous or homozygous mutation in CLCN5 on chromosome Xp11.23. (DO)
Synonyms:exact_synonym: NEPHROLITHIASIS, X-LINKED RECESSIVE;   NPHL1;   Nephrolithiasis 1;   Nephrolithiasis, X-Linked Recessive, Type 1;   Urolithiasis, X-Linked Recessive, Type 1;   X-linked nephrolithiasis with renal failure;   X-linked recessive nephrolithiasis with renal failure;   XRN
 primary_id: MESH:C562901
 alt_id: OMIM:310468
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants           Sort by:
X-linked nephrolithiasis type I term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Clcn5 chloride voltage-gated channel 5 ISO ClinVar Annotator: match by term: Nephrolithiasis, X-linked recessive
ClinVar Annotator: match by term: X-linked recessive nephrolithiasis with renal failure
PMID:8559248 PMID:9602200 PMID:25741868 NCBI chr  X:16,170,585...16,196,691
Ensembl chr  X:16,050,780...16,196,789
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16909
    Nutritional and Metabolic Diseases 5213
      disease of metabolism 5213
        inherited metabolic disorder 2355
          renal tubular transport disease 92
            X-linked nephrolithiasis type I 1
Path 2
Term Annotations click to browse term
  disease 16909
    disease of anatomical entity 16281
      Urogenital Diseases 4199
        urinary system disease 2105
          urolithiasis 62
            nephrolithiasis 46
              calcium oxalate nephrolithiasis 30
                X-linked nephrolithiasis type I 1
paths to the root