Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Pressure injury of ear (disorder) |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic inflammation of postmastoidectomy cavity |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic eustachian salpingitis |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic otitis media |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic petrositis |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic perichondritis of pinna |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic otitis externa |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic mastoiditis |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic tympanitis |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Recurrent acute otitis media |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Benign recurrent vertigo |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic allergic otitis media |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Recurrent labyrinthitis |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Postauricular fistula |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Recurrent vestibulopathy (disorder) |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic eczema of external auditory canal (disorder) |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Furunculosis of external auditory meatus |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic non-suppurative otitis media |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic bacterial otitis externa |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
A rare multiple congenital anomalies syndrome characterized by cutaneous mastocytosis, microcephaly, microtia and/or hearing loss, hypotonia and skeletal anomalies (e.g. clinodactyly, camptodactyly, scoliosis). Additional common features are short stature, intellectual disability and difficulties. Facial dysmorphism may include upslanted palpebral fissures, highly arched palate and micrognathia. Rarely, seizures and asymmetrically small feet have been reported. |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic bilateral vestibulopathy (disorder) |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Persistent left vestibulopathy following vestibular neuronitis (disorder) |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Persistent right vestibulopathy following vestibular neuronitis (disorder) |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic left idiopathic vestibulopathy |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic right idiopathic vestibulopathy (disorder) |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic eustachian tube salpingitis |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Elastotic nodules of antihelix (disorder) |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Neurodermatitis of external ear |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Cauliflower ear |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Seborrheic otitis externa |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Gemignani syndrome is a rare neurodegenerative disease characterized by slowly progressive ataxia, amyotrophy of the hands and distal arms, spastic paraplegia, progressive sensorineural hearing loss, hypogonadism and short stature. Additional features include generalized cerebellar atrophy and peripheral nervous system anomalies. Small cervical spinal cord, intellectual/language disability and localized vitiligo have also been reported. There have been no further descriptions in the literature since 1989. |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome is a rare, syndromic genetic deafness characterized by a combination of muscle weakness, chronic neuropathic and myopathic features, hoarseness and sensorineural hearing loss. A wide range of disease onset and severity has been reported even within the same family. |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Epiphyseal dysplasia-hearing loss-dysmorphism syndrome is a rare multiple congenital anomalies/dysmorphic syndrome characterized by developmental delay, intellectual disability, short stature, sensorineural hearing impairment, facial dysmorphism (including epicanthus, broad, depressed nasal bridge, broad, fleshy nasal tip, mildly anteverted nares, deep nasolabial folds, broad mouth with thin upper lip) and skeletal anomalies (including abnormally placed thumbs, brachydactyly, scoliosis, dysplastic carpal bones). Patients also present severe behavior disturbances (aggression, hyperactivity), as well as hypopigmented skin lesions and hypoplastic digital patterns. There have been no further descriptions in the literature since 1992. |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
A rare primary bone defect, described only in a mother and her three daughters to date, characterized by short stature, hip dislocation, minor vertebral and pelvic changes, and microtia with hearing loss. There have been no further descriptions in the literature since 1981. |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Multiple epiphyseal dysplasia Beighton type (disorder) |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Stapes fixation (stapediovestibular ankylosis) is a hearing loss condition that appears as a consequence of annular ligament destruction followed by excessive connective tissue production during the healing process. This condition is mainly observed in otosclerosis but is also found in chronic otitis media with tympanosclerosis, and other rare bone diseases such as Paget's disease and osteogenesis imperfecta (Lobstein disease). |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic bilateral vestibulopathy due to bilateral schwannoma |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic bilateral vestibulopathy due to and following meningitis (disorder) |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic bilateral vestibulopathy caused by ototoxic agent |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Persistent posttraumatic perforation of ear drum |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Spastic paraplegia-nephritis-deafness syndrome is a complex form of hereditary spastic paraplegia characterized by progressive, variable spastic paraplegia associated with bilateral sensorineural deafness, intellectual disability, and progressive nephropathy. There have been no further descriptions in the literature since 1988. |
Is a |
False |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic deafness |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Cogan's syndrome (disorder) |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by epiphyseal and vertebral dysplasia and abnormalities of the external ears (severe microtia or anotia) and the nose (hypoplastic nose with bifid tip, triangular nares, or anteverted nares). Additional variable findings include short stature, localized aplasia cutis, hypodontia, synophrys, agenesis of the corpus callosum, and cardiac, gastrointestinal, and/or urogenital malformations, among others. Psychomotor development may be delayed. |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|
Chronic seromucinous otitis media |
Is a |
True |
Chronic disease of ear |
Inferred relationship |
Some |
|