autosomal recessive nonsyndromic deafness 35
autosomal recessive nonsyndromic deafness that is characterized severe to profound hearing loss and has material basis in mutation in the ESRRB gene on chromosome 14q24
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autosomal recessive nonsyndromic deafness 35
Summary
autosomal recessive nonsyndromic deafness 35 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 35's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 35's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 35's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 35 is a type of autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 35's genetic association is recorded as ESRRB[6].
- autosomal recessive nonsyndromic deafness 35's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110493[7].
- autosomal recessive nonsyndromic deafness 35's exact match is recorded as http://identifiers.org/doid/DOID:0110493[8].
- autosomal recessive nonsyndromic deafness 35's on focus list of Wikimedia project is recorded as WikiProject Medicine[9].