GenTIGSA Gene Database on Rare Genetic Disorders

Lists of Rare Genetic Disorders  

Familial X-linked Hypophosphatemic Vitamin D Refractory Rickets(X-linked dominant hypophosphatemic rickets)      Explore Disorder's Alias
An X-linked dominant mode(s) within the Bone disorders category
Reported Pathogenic variants
Candidate Gene Information
S.No. Name/GeneID Description Cytogentic Band Gene Location on genomic DNA Gene Length Exons Details Gene Cross-References
1 PHEX/5251 phosphate regulating endopeptidase X-linked Xp22.11 ChrX, NC_000023.11
(22032325..22251310)
218986 nt 26 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

Variant Information    
Disorder Cross-References:      Orphanet          OMIM          GARD          GTR          MedGen          MalaCards          EMBL-EBI OLS    Monarch Initiative          NORD     

Patient care services
Clinical Symptoms & Disabilities