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Namespace Prefixes

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Statements

Subject Item
n2:DOID_0111736
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0050566
rdfs:label
X-linked deafness 3
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obo:id
DOID:0111736
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OMIM:300030
obo:hasExactSynonym
DFN4 congenital sensorineural X-linked deafness 4 DFNX3
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
An X-linked nonsyndromic deafness characterized by congenital, bilateral, profound and sensorineural hearing loss in males and bilateral, mild to moderate high frequency sensorineural hearing impairment with later onset in heterozygous females that has_material_basis_in mutation in a region on chromosome Xp21.2.