amelogenesis imperfecta type 2A1
amelogenesis imperfecta that has material basis in homozygous mutation in the kallikrein-4 gene (KLK4) on chromosome 19q13
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amelogenesis imperfecta type 2A1
Summary
amelogenesis imperfecta type 2A1 is a rare disease[1].
Key Facts
- amelogenesis imperfecta type 2A1's instance of is recorded as rare disease[2].
- amelogenesis imperfecta type 2A1's instance of is recorded as class of disease[3].
- amelogenesis imperfecta type 2A1 is a type of amelogenesis imperfecta[4].
- amelogenesis imperfecta type 2A1 is a type of genetic disease[5].
- amelogenesis imperfecta type 2A1 is a type of autosomal recessive disease[6].
- amelogenesis imperfecta type 2A1's health specialty is recorded as gastroenterology[7].
- amelogenesis imperfecta type 2A1's genetic association is recorded as KLK4[8].
- amelogenesis imperfecta type 2A1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110057[9].
- amelogenesis imperfecta type 2A1's exact match is recorded as http://identifiers.org/doid/DOID:0110057[10].
- amelogenesis imperfecta type 2A1's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].