Concept information
Preferred term
Congenital sensorineural hearing loss (disorder)
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Narrower concepts
- Albinism-deafness syndrome of Tietz (disorder)
- Albinism with deafness syndrome (disorder)
- Bartter syndrome type 4
- Bosley Salih Alorainy syndrome (disorder)
- Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome
- Congenital cataract, hearing loss, severe developmental delay syndrome (disorder)
- Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome
- Congenital cataract with deafness and hypogonadism syndrome (disorder)
- Congenital mixed conductive and sensorineural hearing loss
- Craniofacial deafness hand syndrome (disorder)
- Deafness and intellectual disability Martin Probst type syndrome (disorder)
- Deafness and oligodontia syndrome (disorder)
- Deafness, small bowel diverticulosis, neuropathy syndrome (disorder)
- Deafness with epiphyseal dysplasia and short stature syndrome (disorder)
- Deafness with onychodystrophy syndrome
- Deafness with skeletal dysplasia and lip granuloma syndrome (disorder)
- Finucane Kurtz Scott syndrome
- Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome (disorder)
- Isolated prelingual genetic deafness
- Keipert syndrome (disorder)
- Lowry Yong syndrome
- MDP (mandibular hypoplasia, deafness, progeroid) syndrome
- Myoclonus, cerebellar ataxia, deafness syndrome
- Ocular albinism with congenital sensorineural deafness
- Oculootodental syndrome
- Rubella deafness
- Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome (disorder)
- Spastic paraplegia, nephritis, deafness syndrome (disorder)
- Stickler syndrome non-ocular type
- Temtamy preaxial brachydactyly syndrome
- Wildervanck's syndrome
Finding site
Interprets
Is a
- 60700002
- 95827002
Occurrence
In other languages
URI
http://www.irandoc.acir/onto/irandoc/700453005
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