primary coenzyme Q10 deficiency 2
primary coenzyme Q10 deficiency that has material basis in an autosomal recessive mutation of PDSS1 on chromosome 10p12.1
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primary coenzyme Q10 deficiency 2
Summary
primary coenzyme Q10 deficiency 2 is a rare disease[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- primary coenzyme Q10 deficiency 2's instance of is recorded as rare disease[3].
- primary coenzyme Q10 deficiency 2's instance of is recorded as class of disease[4].
- primary coenzyme Q10 deficiency 2 is a type of coenzyme Q10 deficiency disease[5].
- primary coenzyme Q10 deficiency 2 is a type of genetic disease[6].
- primary coenzyme Q10 deficiency 2's genetic association is recorded as PDSS1[7].
- primary coenzyme Q10 deficiency 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070239[8].
- primary coenzyme Q10 deficiency 2's exact match is recorded as http://identifiers.org/doid/DOID:0070239[9].
- primary coenzyme Q10 deficiency 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].
Why It Matters
primary coenzyme Q10 deficiency 2 is known by 5 alternative names across languages and contexts.[2]