Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
surdité d'une oreille |
Is a |
False |
Hearing loss |
Inferred relationship |
Some |
|
Partial deafness |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Noise effects on inner ear |
Is a |
False |
Hearing loss |
Inferred relationship |
Some |
|
Psychogenic deafness |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Toxic deafness |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Paradoxic hearing loss |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Conductive hearing loss |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
surdité pour fréquences hautes |
Is a |
False |
Hearing loss |
Inferred relationship |
Some |
|
Jervell and Lange-Nielson syndrome |
Is a |
False |
Hearing loss |
Inferred relationship |
Some |
|
Tone deafness |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Sensorineural hearing loss |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Deaf mutism |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Sudden hearing loss |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Complete deafness |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Traumatic deafness |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
perte d'audition unilatérale |
Is a |
False |
Hearing loss |
Inferred relationship |
Some |
|
Bilateral hearing loss |
Is a |
False |
Hearing loss |
Inferred relationship |
Some |
|
Neonatal hearing loss |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Transient ischemic deafness |
Is a |
False |
Hearing loss |
Inferred relationship |
Some |
|
surdité unilatérale |
Is a |
False |
Hearing loss |
Inferred relationship |
Some |
|
Bilateral deafness |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Chronic deafness |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
symptôme de surdité |
Is a |
False |
Hearing loss |
Inferred relationship |
Some |
|
FH: Deafness |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
1 |
On examination - slightly deaf |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
1 |
à l'examen : significativement sourd |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
1 |
On examination - very deaf |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
1 |
Ear anomalies with hearing impairment |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
|
à l'examen : sourd |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
1 |
Ear anomalies with hearing impaired, unspecified |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
|
Ear anomaly with hearing impaired NOS |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
|
Deafness due to congenital anomaly NEC |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
|
Other and unspecified ear anomaly with hearing impaired |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
|
Deafness suspected |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
1 |
Noise-induced hearing loss |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
à l'examen : significativement sourd |
Is a |
False |
Hearing loss |
Inferred relationship |
Some |
|
à l'examen : sourd |
Is a |
False |
Hearing loss |
Inferred relationship |
Some |
|
Asymmetrical hearing loss (disorder) |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Combined visual and hearing impairment (disorder) |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Deafness suspected |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
1 |
FH: Deafness |
Associated finding |
True |
Hearing loss |
Inferred relationship |
Some |
1 |
Family history of hearing loss (situation) |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
1 |
Family history of hearing loss (situation) |
Associated finding |
True |
Hearing loss |
Inferred relationship |
Some |
1 |
Speech and language developmental delay due to hearing loss (disorder) |
Due to |
True |
Hearing loss |
Inferred relationship |
Some |
1 |
FH: Father deaf |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
1 |
surdité unilatérale |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
1 |
perte d'audition unilatérale |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
1 |
FH: Deafness |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
1 |
Family history of hearing loss (situation) |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
1 |
surdité unilatérale |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
1 |
perte d'audition unilatérale |
Associated finding |
False |
Hearing loss |
Inferred relationship |
Some |
1 |
History of hearing loss |
Associated finding |
True |
Hearing loss |
Inferred relationship |
Some |
1 |
No history of hearing loss |
Associated finding |
True |
Hearing loss |
Inferred relationship |
Some |
1 |
Hearing loss of right ear (disorder) |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Hearing loss of left ear (disorder) |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Congenital anomaly of ear with impairment of hearing |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Mild to moderate hearing loss |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Severe hearing loss |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Screening for hearing loss (procedure) |
Has focus |
True |
Hearing loss |
Inferred relationship |
Some |
2 |
Deafness-craniofacial syndrome is characterized by the association of congenital hearing loss and facial dysmorphism (facial asymmetry, a broad nasal root and small nasal alae). It has been described in two members (father and daughter) of one Jewish family. Temporal alopecia was also noted. Transmission appeared to be autosomal dominant. |
Is a |
False |
Hearing loss |
Inferred relationship |
Some |
|
Microcephaly-deafness-intellectual disability syndrome is characterized by microcephaly, deafness, intellectual deficit and facial dysmorphism (facial asymmetry, prominent glabella, low-set and cup-shaped ears, protruding lower lip, micrognathia). It has been described in a mother and her son. The mode of inheritance is probably autosomal dominant. |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Orofaciodigital syndrome type 11 is an extremely rare, sporadic form of Orofaciodigital syndrome with only a few reported cases, and characterized by facial (blepharophimosis, bulbous nasal tip, broad nasal bridge, downslanting palpebral fissures and low set ears) and skeletal (post-axial polydactyly and fusion of vertebrae) malformations along with severe intellectual disability, deafness and congenital heart defects. |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Acquired hearing loss (disorder) |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Birth trauma deafness |
Is a |
False |
Hearing loss |
Inferred relationship |
Some |
|
Robinson nail dystrophy-deafness syndrome |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
A rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by moderate to severe intellectual disability, congenital aphonia, hearing loss, optic atrophy, retinal dystrophy, broad thumbs and duplicated halluces. Facial dysmorphism (including thick eyebrows, ptosis, long, downslanting palpebral fissures, microstomia, low-set, posteriorly rotated ears) and genital abnormalities are also associated. |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Transient ischaemic deafness |
Is a |
False |
Hearing loss |
Inferred relationship |
Some |
|
Lethal ataxia with deafness and optic atrophy (also known as Arts syndrome) is characterised by intellectual deficit, early-onset hypotonia, ataxia, delayed motor development, hearing impairment and loss of vision due to optic atrophy. |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Hearing loss associated with syndrome |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Hystrix ichthyosis with deafness |
Is a |
False |
Hearing loss |
Inferred relationship |
Some |
|
Melnick-Fraser syndrome |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
A rare neurologic disease characterized by spastic paraparesis presenting in late childhood and hearing loss. Additional features may include retinal anomalies, lenticular opacities, short stature, hypogonadism, sensory deficits, tremor, dysdiadochokinesia, elevated cerebrospinal fluid protein, and absent or prolonged somatosensory evoked potentials. Plasma and fibroblast levels of saturated very long-chain fatty acids are normal. There have been no further descriptions in the literature since 1986. |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Education for hearing impairment (procedure) |
Has focus |
True |
Hearing loss |
Inferred relationship |
Some |
2 |
Transitory deafness |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
A very rare lysosomal storage disease with characteristics of developmental delay of varying severity and hearing loss, but that can manifest a wide phenotypic heterogeneity. |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Profound hearing loss |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|
Deafness is the most frequent form of sensorial deficit. In the vast majority of cases, the deafness is termed nonsyndromic or isolated and the hearing loss is the only clinical anomaly reported. In developed counties, 60-80% of cases of early-onset hearing loss are of genetic origin. |
Is a |
True |
Hearing loss |
Inferred relationship |
Some |
|