released
October 28th, 2019 at 9:28pm
Details
Details
namespace
http://purl.obolibrary.org/obo
parents
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- Mitochondrial disorder due to a defect in assembly or maturation of the respiratory chain complexes
- autosomal recessive disease
- Syndromic genetic deafness
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preferred_name
auditory neuropathy and optic atrophy
source_ontologies
term_id
MONDO:0060582
term_name
auditory neuropathy-optic atrophy syndrome
term_url
http://purl.obolibrary.org/obo/MONDO_0060582