Disease #02043 (pyropoikilocytosis, hereditary, OMIM:266140)

Official abbreviation -
Name pyropoikilocytosis, hereditary
OMIM ID 266140
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene SPTA1
Associated tissues -
Disease features -
Remarks -