Disease #02608 (FMRD (deficiency, fumarase (FMRD)), OMIM:606812)

Official abbreviation FMRD
Name deficiency, fumarase (FMRD)
OMIM ID 606812
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene FH
Associated tissues -
Disease features -
Remarks -

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