Chain1043: Mitochondrial HMG-CoA Synthase Deficiency

This is a rare disease.

Example use A

Rare disease screening of newborns or adults thinking of having children. Could also be used as part of a comprehensive analysis of a person's genes.

Developer

Dr. Colby

Genetic info

GenesGenetic variants
HMGCS2chr1:120302538,chr1:120293453

Qualitative

Type

text

Possible responses

Carrier, Possibly Affected, Not Detected, insufficient data, error