Disease #05255 (SHPKD (deficiency, sedoheptulokinase (SHPKD)), OMIM:617213)

Official abbreviation SHPKD
Name deficiency, sedoheptulokinase (SHPKD)
OMIM ID 617213
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene SHPK
Associated tissues -
Disease features -
Remarks -