ACTIONABILITY KNOWLEDGE REPOSITORY ACTIONABILITY CURATION INTERFACE

Adult Summary Report Secondary Findings in Adult Subjects Non-diagnostic, excludes newborn screening & prenatal testing/screening A Current Version Rule-Out Dashboard Release History Status (Adult): Incomplete (Consensus scoring is Incomplete) Curation Status (Adult): Released - Under Revision 2.0.1 Status (Pediatric): Passed (Consensus scoring is Complete) P

GENE/GENE PANEL: MUT, MMAA, MMAB, MMADHC, MCEE
Condition: Methylmalonic Acidemia
Mode(s) of Inheritance: Autosomal Recessive
Actionability Assertion
Gene Condition Pairs(s)
Final Assertion
MUT251000 (methylmalonic aciduria due to methylmalonyl-coa mutase deficiency)
N/A - Insufficient evidence: early rule-out
MMAA251100 (methylmalonic aciduria, cbla type)
N/A - Insufficient evidence: early rule-out
MMAB251110 (methylmalonic aciduria, cblb type)
N/A - Insufficient evidence: early rule-out
MMADHC277410 (methylmalonic aciduria and homocystinuria, cbld type; mahcd)
N/A - Insufficient evidence: early rule-out
MCEE251120 (methylmalonyl-coa epimerase deficiency)
N/A - Insufficient evidence: early rule-out
NOTICE
The 'Stage 2 Summary Report' is not available because at this version,
this gene-disease pair did not pass the Stage 1 Rule-Out survey.
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