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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