primary coenzyme Q10 deficiency 5
primary coenzyme Q10 deficiency that has material basis in an autosomal recessive mutation of COQ9 on chromosome 16q21
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primary coenzyme Q10 deficiency 5
Summary
primary coenzyme Q10 deficiency 5 is a rare disease[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- primary coenzyme Q10 deficiency 5's instance of is recorded as rare disease[3].
- primary coenzyme Q10 deficiency 5's instance of is recorded as class of disease[4].
- primary coenzyme Q10 deficiency 5 is a type of coenzyme Q10 deficiency disease[5].
- primary coenzyme Q10 deficiency 5 is a type of genetic disease[6].
- primary coenzyme Q10 deficiency 5's genetic association is recorded as COQ9[7].
- primary coenzyme Q10 deficiency 5's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070242[8].
- primary coenzyme Q10 deficiency 5's exact match is recorded as http://identifiers.org/doid/DOID:0070242[9].
- primary coenzyme Q10 deficiency 5's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].
Why It Matters
primary coenzyme Q10 deficiency 5 is known by 5 alternative names across languages and contexts.[2]