Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Congenital aplasia of inner ear |
Is a |
True |
Congenital anomaly of inner ear |
Inferred relationship |
Some |
|
Neurofibromatosis type 2 |
Is a |
False |
Congenital anomaly of inner ear |
Inferred relationship |
Some |
|
Congenital abnormal shape of inner ear |
Is a |
True |
Congenital anomaly of inner ear |
Inferred relationship |
Some |
|
Congenital deafness |
Is a |
False |
Congenital anomaly of inner ear |
Inferred relationship |
Some |
|
Hutchinson's triad |
Is a |
False |
Congenital anomaly of inner ear |
Inferred relationship |
Some |
|
Structural anomaly of the cochlea and vestibular labyrinth |
Is a |
True |
Congenital anomaly of inner ear |
Inferred relationship |
Some |
|
Vascular malformation of inner ear |
Is a |
True |
Congenital anomaly of inner ear |
Inferred relationship |
Some |
|
Congenital anomaly of membranous labyrinth |
Is a |
False |
Congenital anomaly of inner ear |
Inferred relationship |
Some |
|
Inner ear anomalies NOS |
Is a |
False |
Congenital anomaly of inner ear |
Inferred relationship |
Some |
|
Deafness-vitiligo-achalasia syndrome is characterized by the association of deafness, short stature, vitiligo, muscle wasting, and achalasia. |
Is a |
True |
Congenital anomaly of inner ear |
Inferred relationship |
Some |
|
Deafness with labyrinthine aplasia, microtia, and microdontia (LAMM) is a genetic transmission deafness syndrome. |
Is a |
True |
Congenital anomaly of inner ear |
Inferred relationship |
Some |
|
A rare, genetic, hematologic disorder characterized by bone marrow failure which manifests with aplastic anemia and/or myelodysplasia, associated with hearing/ear abnormalities (such as deafness, labyrinthitis), inherited in an autosomal dominant manner. |
Is a |
True |
Congenital anomaly of inner ear |
Inferred relationship |
Some |
|
Neutropenia-monocytopenia-deafness syndrome is characterized by neutropenia with myeloid marrow hypoplasia, monocytopenia, and congenital deafness. It has been described in three siblings who suffered recurrent bacterial infections. |
Is a |
True |
Congenital anomaly of inner ear |
Inferred relationship |
Some |
|
Sinoatrial node dysfunction and deafness is a rare genetic disease characterized by congenital severe to profound deafness with no evidence of vestibular dysfunction, associated with sinoatrial node dysfunction with pronounced bradycardia and increased variability of heart rate at rest and episodic syncopes that may be triggered by enhanced physical activity and stress. |
Is a |
True |
Congenital anomaly of inner ear |
Inferred relationship |
Some |
|
A rare otorhinolaryngological malformation characterized by varying degrees of malformation of the inner ear associated with severe to profound congenital sensorineural hearing loss in the absence of cochlear nerve anomalies (hypoplasia or aplasia). Categorization of the malformation is based on the morphology of the cochlea, modiolus, and lamina cribrosa, which can range from normal development of these structures (with the malformation being limited to other structures of the inner ear) to their complete absence. |
Is a |
True |
Congenital anomaly of inner ear |
Inferred relationship |
Some |
|