multiple mitochondrial dysfunctions syndrome 1

Summary

multiple mitochondrial dysfunctions syndrome 1 is a developmental defect during embryogenesis^[1]. It is known by 6 alternative names across languages and contexts.^[2]

Key Facts

• multiple mitochondrial dysfunctions syndrome 1's instance of is recorded as developmental defect during embryogenesis^[3].
• multiple mitochondrial dysfunctions syndrome 1's instance of is recorded as rare disease^[4].
• multiple mitochondrial dysfunctions syndrome 1's instance of is recorded as class of disease^[5].
• multiple mitochondrial dysfunctions syndrome 1 is a type of autosomal recessive disease^[6].
• multiple mitochondrial dysfunctions syndrome 1 is a type of fatal multiple mitochondrial dysfunctions syndrome^[7].
• multiple mitochondrial dysfunctions syndrome 1's genetic association is recorded as NFU1^[8].
• multiple mitochondrial dysfunctions syndrome 1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080133^[9].
• multiple mitochondrial dysfunctions syndrome 1's exact match is recorded as http://identifiers.org/doid/DOID:0080133^[10].
• multiple mitochondrial dysfunctions syndrome 1's on focus list of Wikimedia project is recorded as WikiProject Medicine^[11].

Why It Matters

multiple mitochondrial dysfunctions syndrome 1 is known by 6 alternative names across languages and contexts.^[2]