amelogenesis imperfecta type 1H
amelogenesis imperfecta that has material basis in homozygous or compound heterozygous mutation in the integrin beta-6 gene (ITGB6) on chromosome 2q24
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amelogenesis imperfecta type 1H
Summary
amelogenesis imperfecta type 1H is a rare disease[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- amelogenesis imperfecta type 1H's instance of is recorded as rare disease[3].
- amelogenesis imperfecta type 1H's instance of is recorded as class of disease[4].
- amelogenesis imperfecta type 1H is a type of amelogenesis imperfecta[5].
- amelogenesis imperfecta type 1H is a type of hypoplastic amelogenesis imperfecta[6].
- amelogenesis imperfecta type 1H is a type of autosomal recessive disease[7].
- amelogenesis imperfecta type 1H's health specialty is recorded as gastroenterology[8].
- amelogenesis imperfecta type 1H's genetic association is recorded as ITGB6[9].
- amelogenesis imperfecta type 1H's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110064[10].
- amelogenesis imperfecta type 1H's exact match is recorded as http://identifiers.org/doid/DOID:0110064[11].
- amelogenesis imperfecta type 1H's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
Why It Matters
amelogenesis imperfecta type 1H is known by 5 alternative names across languages and contexts.[2]