multiple mitochondrial dysfunctions syndrome 4

Summary

multiple mitochondrial dysfunctions syndrome 4 is a developmental defect during embryogenesis^[1]. It is known by 4 alternative names across languages and contexts.^[2]

Key Facts

• multiple mitochondrial dysfunctions syndrome 4's instance of is recorded as developmental defect during embryogenesis^[3].
• multiple mitochondrial dysfunctions syndrome 4's instance of is recorded as rare disease^[4].
• multiple mitochondrial dysfunctions syndrome 4's instance of is recorded as class of disease^[5].
• multiple mitochondrial dysfunctions syndrome 4 is a type of nervous system heredodegenerative disease^[6].
• multiple mitochondrial dysfunctions syndrome 4 is a type of eye degenerative disease^[7].
• multiple mitochondrial dysfunctions syndrome 4 is a type of syndromic hereditary optic neuropathy^[8].
• multiple mitochondrial dysfunctions syndrome 4 is a type of autosomal recessive disease^[9].
• multiple mitochondrial dysfunctions syndrome 4 is a type of fatal multiple mitochondrial dysfunctions syndrome^[10].
• multiple mitochondrial dysfunctions syndrome 4's genetic association is recorded as ISCA2^[11].
• multiple mitochondrial dysfunctions syndrome 4's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080136^[12].
• multiple mitochondrial dysfunctions syndrome 4's exact match is recorded as http://identifiers.org/doid/DOID:0080136^[13].
• multiple mitochondrial dysfunctions syndrome 4's on focus list of Wikimedia project is recorded as WikiProject Medicine^[14].

Why It Matters

multiple mitochondrial dysfunctions syndrome 4 is known by 4 alternative names across languages and contexts.^[2]