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Multiple mitochondrial dysfunctions syndrome 9b(MMDS9B)

MedGen UID:
1860851
Concept ID:
C5935635
Disease or Syndrome
Synonyms: MMDS9B; MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 9B
 
Gene (location): FDXR (17q25.1)
 
Monarch Initiative: MONDO:0971174
OMIM®: 620887

Definition

Multiple mitochondrial dysfunctions syndrome-9B (MMDS9B) is characterized by optic atrophy and/or auditory neuropathy variably associated with developmental delay or regression, global hypotonia, pyramidal and cerebellar signs, and seizures (summary by Masnada et al., 2023). [from OMIM]

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