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's subclass of is recorded as amelogenesis imperfecta[4].
- amelogenesis imperfecta type 1F's subclass of is recorded as hypoplastic amelogenesis imperfecta[5].
- amelogenesis imperfecta type 1F's subclass of is recorded as autosomal recessive disease[6].
- amelogenesis imperfecta type 1F's OMIM ID is recorded as 616270[7].
- amelogenesis imperfecta type 1F's Disease Ontology ID is recorded as DOID:0110065[8].
- amelogenesis imperfecta type 1F's health specialty is recorded as gastroenterology[9].
- amelogenesis imperfecta type 1F's genetic association is recorded as AMBN[10].
- amelogenesis imperfecta type 1F's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110065[11].
- amelogenesis imperfecta type 1F's exact match is recorded as http://identifiers.org/doid/DOID:0110065[12].
- amelogenesis imperfecta type 1F's UMLS CUI is recorded as C4225394[13].
- amelogenesis imperfecta type 1F's ICD-10-CM is recorded as K00.5[14].
- amelogenesis imperfecta type 1F's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- amelogenesis imperfecta type 1F's Mondo ID is recorded as MONDO_0014560[16].
- amelogenesis imperfecta type 1F's UniProt disease ID is recorded as DI-04358[17].