autosomal recessive nonsyndromic deafness 28
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the TRIOBP gene on chromosome 22q13
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Summary
autosomal recessive nonsyndromic deafness 28 is a head and neck disease[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- autosomal recessive nonsyndromic deafness 28's instance of is recorded as head and neck disease[3].
- autosomal recessive nonsyndromic deafness 28's instance of is recorded as rare disease[4].
- autosomal recessive nonsyndromic deafness 28's instance of is recorded as class of disease[5].
- autosomal recessive nonsyndromic deafness 28 is a type of autosomal recessive nonsyndromic deafness[6].
- autosomal recessive nonsyndromic deafness 28's NCI Thesaurus ID is recorded as C129023[7].
- autosomal recessive nonsyndromic deafness 28's genetic association is recorded as TRIOBP[8].
- autosomal recessive nonsyndromic deafness 28's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110486[9].
- autosomal recessive nonsyndromic deafness 28's exact match is recorded as http://identifiers.org/doid/DOID:0110486[10].
- autosomal recessive nonsyndromic deafness 28's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
Why It Matters
autosomal recessive nonsyndromic deafness 28 is known by 7 alternative names across languages and contexts.[2]