autosomal dominant nonsyndromic deafness 41
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat progressive hearing loss and has material basis in mutation in the P2RX2 gene on chromosome 12q24
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Summary
autosomal dominant nonsyndromic deafness 41 is a head and neck disease[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- autosomal dominant nonsyndromic deafness 41's instance of is recorded as head and neck disease[3].
- autosomal dominant nonsyndromic deafness 41's instance of is recorded as rare disease[4].
- autosomal dominant nonsyndromic deafness 41's instance of is recorded as class of disease[5].
- autosomal dominant nonsyndromic deafness 41 is a type of autosomal dominant nonsyndromic deafness[6].
- autosomal dominant nonsyndromic deafness 41's NCI Thesaurus ID is recorded as C175700[7].
- autosomal dominant nonsyndromic deafness 41's genetic association is recorded as P2RX2[8].
- autosomal dominant nonsyndromic deafness 41's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110567[9].
- autosomal dominant nonsyndromic deafness 41's exact match is recorded as http://identifiers.org/doid/DOID:0110567[10].
- autosomal dominant nonsyndromic deafness 41's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
Why It Matters
autosomal dominant nonsyndromic deafness 41 is known by 7 alternative names across languages and contexts.[2]