Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Hearing for whisper impaired |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Hearing for conversational voice impaired |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Hearing for loud voice impaired |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Hearing for voice impaired |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Finding related to ability to hear voice abnormal |
est un(e) (attribut) |
False |
Decreased hearing |
Inferred relationship |
Some |
|
Unable to hear whisper |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Unable to hear conversational voice |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Unable to hear loud voice |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Cutaneous mastocytosis, short stature, hearing loss syndrome (disorder) |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Beta-D-mannosidosis |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Ocular albinism with congenital sensorineural deafness |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Autosomal dominant spastic paraplegia type 29 (disorder) |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Spastic paraplegia, nephritis, deafness syndrome (disorder) |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Congenital ichthyosis, microcephalus, tetraplegia syndrome (disorder) |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Stickler syndrome type 3 (disorder) |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Deafness with onychodystrophy syndrome |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy (disorder) |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Auditory neuropathy, optic atrophy syndrome (disorder) |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome (disorder) |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
PCNA-related progressive neurodegenerative photosensitivity syndrome |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome (disorder) |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Duane retraction syndrome with congenital deafness |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Deafness, enamel hypoplasia, nail defect syndrome (disorder) |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Congenital cochleovestibular malformation |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Hearing difficulty |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|
Hearing loss remits during vertigo attacks |
est un(e) (attribut) |
False |
Decreased hearing |
Inferred relationship |
Some |
|
Congenital conductive hearing loss |
est un(e) (attribut) |
True |
Decreased hearing |
Inferred relationship |
Some |
|