amelogenesis imperfecta type 1G
amelogenesis imperfecta that has material basis in homozygous or compound heterozygous mutation in the FAM20A gene on chromosome 17q24
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amelogenesis imperfecta type 1G
Summary
amelogenesis imperfecta type 1G is a developmental defect during embryogenesis[1]. It draws 4 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #132 of 308).[2]
Key Facts
- amelogenesis imperfecta type 1G's instance of is recorded as developmental defect during embryogenesis[3].
- amelogenesis imperfecta type 1G's instance of is recorded as rare disease[4].
- amelogenesis imperfecta type 1G's instance of is recorded as class of disease[5].
- amelogenesis imperfecta type 1G is a type of amelogenesis imperfecta[6].
- amelogenesis imperfecta type 1G is a type of nephropathy secondary to a storage or other metabolic disease[7].
- amelogenesis imperfecta type 1G is a type of rare genetic developmental defect during embryogenesis[8].
- amelogenesis imperfecta type 1G is a type of malformation syndrome with odontal and/or periodontal component[9].
- amelogenesis imperfecta type 1G is a type of autosomal recessive disease[10].
- amelogenesis imperfecta type 1G's ICD-9-CM is recorded as 520.5[11].
- amelogenesis imperfecta type 1G's health specialty is recorded as gastroenterology[12].
- amelogenesis imperfecta type 1G's genetic association is recorded as FAM20A[13].
- amelogenesis imperfecta type 1G's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110066[14].
- amelogenesis imperfecta type 1G's exact match is recorded as http://identifiers.org/doid/DOID:0110066[15].
- amelogenesis imperfecta type 1G's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
amelogenesis imperfecta type 1G draws 4 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #132 of 308).[2] It is known by 14 alternative names across languages and contexts.[17]