amelogenesis imperfecta hypomaturation type 2A2
amelogenesis imperfecta that has material basis in homozygous mutation in the matrix metalloproteinase-20 gene (MMP20)
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amelogenesis imperfecta hypomaturation type 2A2
Summary
amelogenesis imperfecta hypomaturation type 2A2 is a rare disease[1].
Key Facts
- amelogenesis imperfecta hypomaturation type 2A2's instance of is recorded as rare disease[2].
- amelogenesis imperfecta hypomaturation type 2A2's instance of is recorded as class of disease[3].
- amelogenesis imperfecta hypomaturation type 2A2's subclass of is recorded as amelogenesis imperfecta[4].
- amelogenesis imperfecta hypomaturation type 2A2's subclass of is recorded as autosomal recessive disease[5].
- amelogenesis imperfecta hypomaturation type 2A2's MeSH descriptor ID is recorded as C567279[6].
- amelogenesis imperfecta hypomaturation type 2A2's OMIM ID is recorded as 612529[7].
- amelogenesis imperfecta hypomaturation type 2A2's Disease Ontology ID is recorded as DOID:0110060[8].
- amelogenesis imperfecta hypomaturation type 2A2's health specialty is recorded as gastroenterology[9].
- amelogenesis imperfecta hypomaturation type 2A2's genetic association is recorded as MMP20[10].
- amelogenesis imperfecta hypomaturation type 2A2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110060[11].
- amelogenesis imperfecta hypomaturation type 2A2's exact match is recorded as http://identifiers.org/doid/DOID:0110060[12].
- amelogenesis imperfecta hypomaturation type 2A2's UMLS CUI is recorded as C2675858[13].
- amelogenesis imperfecta hypomaturation type 2A2's ICD-10-CM is recorded as K00.5[14].
- amelogenesis imperfecta hypomaturation type 2A2's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- amelogenesis imperfecta hypomaturation type 2A2's Mondo ID is recorded as MONDO_0012926[16].
- amelogenesis imperfecta hypomaturation type 2A2's UniProt disease ID is recorded as DI-00092[17].