combined oxidative phosphorylation defect type 25

Summary

combined oxidative phosphorylation defect type 25 is a head and neck disease^[1]. It is known by 5 alternative names across languages and contexts.^[2]

Key Facts

• combined oxidative phosphorylation defect type 25's instance of is recorded as head and neck disease^[3].
• combined oxidative phosphorylation defect type 25's instance of is recorded as developmental defect during embryogenesis^[4].
• combined oxidative phosphorylation defect type 25's instance of is recorded as rare disease^[5].
• combined oxidative phosphorylation defect type 25's instance of is recorded as class of disease^[6].
• combined oxidative phosphorylation defect type 25 is a type of neurometabolic disease^[7].
• combined oxidative phosphorylation defect type 25 is a type of syndromic genetic deafness^[8].
• combined oxidative phosphorylation defect type 25 is a type of combined oxidative phosphorylation deficiency^[9].
• combined oxidative phosphorylation defect type 25 is a type of autosomal recessive disease^[10].
• combined oxidative phosphorylation defect type 25's genetic association is recorded as MARS2^[11].
• combined oxidative phosphorylation defect type 25's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_447954^[12].
• combined oxidative phosphorylation defect type 25's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111468^[13].
• combined oxidative phosphorylation defect type 25's exact match is recorded as http://identifiers.org/doid/DOID:0111468^[14].

Why It Matters

combined oxidative phosphorylation defect type 25 is known by 5 alternative names across languages and contexts.^[2]