amelogenesis imperfecta type 1F
amelogenesis imperfecta that has material basis in homozygous mutation in the ameloblastin gene (AMBN) on chromosome 4q13
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amelogenesis imperfecta type 1F
Summary
amelogenesis imperfecta type 1F is a rare disease[1].
Key Facts
- amelogenesis imperfecta type 1F's instance of is recorded as rare disease[2].
- amelogenesis imperfecta type 1F's instance of is recorded as class of disease[3].
- amelogenesis imperfecta type 1F is a type of amelogenesis imperfecta[4].
- amelogenesis imperfecta type 1F is a type of hypoplastic amelogenesis imperfecta[5].
- amelogenesis imperfecta type 1F is a type of autosomal recessive disease[6].
- amelogenesis imperfecta type 1F's health specialty is recorded as gastroenterology[7].
- amelogenesis imperfecta type 1F's genetic association is recorded as AMBN[8].
- amelogenesis imperfecta type 1F's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110065[9].
- amelogenesis imperfecta type 1F's exact match is recorded as http://identifiers.org/doid/DOID:0110065[10].
- amelogenesis imperfecta type 1F's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].