multiple mitochondrial dysfunctions syndrome 5
human disease
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multiple mitochondrial dysfunctions syndrome 5
Summary
multiple mitochondrial dysfunctions syndrome 5 is a developmental defect during embryogenesis[1]. It is known by 3 alternative names across languages and contexts.[2]
Key Facts
- multiple mitochondrial dysfunctions syndrome 5's instance of is recorded as developmental defect during embryogenesis[3].
- multiple mitochondrial dysfunctions syndrome 5's instance of is recorded as class of disease[4].
- multiple mitochondrial dysfunctions syndrome 5 is a type of autosomal recessive disease[5].
- multiple mitochondrial dysfunctions syndrome 5 is a type of fatal multiple mitochondrial dysfunctions syndrome[6].
- multiple mitochondrial dysfunctions syndrome 5's genetic association is recorded as ISCA1[7].
- multiple mitochondrial dysfunctions syndrome 5's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080274[8].
- multiple mitochondrial dysfunctions syndrome 5's exact match is recorded as http://identifiers.org/doid/DOID:0080274[9].
- multiple mitochondrial dysfunctions syndrome 5's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].
Why It Matters
multiple mitochondrial dysfunctions syndrome 5 is known by 3 alternative names across languages and contexts.[2]