mitochondrial DNA depletion syndrome 1
Human disease
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mitochondrial DNA depletion syndrome 1
Summary
mitochondrial DNA depletion syndrome 1 is a developmental defect during embryogenesis[1]. It is known by 12 alternative names across languages and contexts.[2]
Key Facts
- mitochondrial DNA depletion syndrome 1's instance of is recorded as developmental defect during embryogenesis[3].
- mitochondrial DNA depletion syndrome 1's instance of is recorded as rare disease[4].
- mitochondrial DNA depletion syndrome 1's instance of is recorded as class of disease[5].
- mitochondrial DNA depletion syndrome 1 is a type of mitochondrial DNA depletion syndrome[6].
- mitochondrial DNA depletion syndrome 1 is a type of autosomal recessive disease[7].
- mitochondrial DNA depletion syndrome 1's symptoms and signs is recorded as ptosis[8].
- mitochondrial DNA depletion syndrome 1's NCI Thesaurus ID is recorded as C11967[9].
- mitochondrial DNA depletion syndrome 1's genetic association is recorded as TYMP[10].
- mitochondrial DNA depletion syndrome 1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080119[11].
- mitochondrial DNA depletion syndrome 1's exact match is recorded as http://identifiers.org/doid/DOID:0080119[12].
- mitochondrial DNA depletion syndrome 1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_298[13].
- mitochondrial DNA depletion syndrome 1's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
mitochondrial DNA depletion syndrome 1 is known by 12 alternative names across languages and contexts.[2]