amelogenesis imperfecta hypomaturation type 2A3
amelogenesis imperfecta caused by homozygous mutation in the WDR72 gene
Press Enter · cited answer in seconds
0 sources
amelogenesis imperfecta hypomaturation type 2A3
Summary
amelogenesis imperfecta hypomaturation type 2A3 is a rare disease[1].
Key Facts
- amelogenesis imperfecta hypomaturation type 2A3's instance of is recorded as rare disease[2].
- amelogenesis imperfecta hypomaturation type 2A3's instance of is recorded as class of disease[3].
- amelogenesis imperfecta hypomaturation type 2A3's subclass of is recorded as amelogenesis imperfecta[4].
- amelogenesis imperfecta hypomaturation type 2A3's subclass of is recorded as autosomal recessive disease[5].
- amelogenesis imperfecta hypomaturation type 2A3's MeSH descriptor ID is recorded as C567706[6].
- amelogenesis imperfecta hypomaturation type 2A3's OMIM ID is recorded as 613211[7].
- amelogenesis imperfecta hypomaturation type 2A3's Disease Ontology ID is recorded as DOID:0110061[8].
- amelogenesis imperfecta hypomaturation type 2A3's health specialty is recorded as gastroenterology[9].
- amelogenesis imperfecta hypomaturation type 2A3's genetic association is recorded as WDR72[10].
- amelogenesis imperfecta hypomaturation type 2A3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110061[11].
- amelogenesis imperfecta hypomaturation type 2A3's exact match is recorded as http://identifiers.org/doid/DOID:0110061[12].
- amelogenesis imperfecta hypomaturation type 2A3's UMLS CUI is recorded as C2750771[13].
- amelogenesis imperfecta hypomaturation type 2A3's ICD-10-CM is recorded as K00.5[14].
- amelogenesis imperfecta hypomaturation type 2A3's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- amelogenesis imperfecta hypomaturation type 2A3's Mondo ID is recorded as MONDO_0013181[16].
- amelogenesis imperfecta hypomaturation type 2A3's UniProt disease ID is recorded as DI-02570[17].