amelogenesis imperfecta hypomaturation type 2A4
amelogenesis imperfecta caused by homozygous mutation in the C4ORF26 gene on chromosome 4q21
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amelogenesis imperfecta hypomaturation type 2A4
Summary
amelogenesis imperfecta hypomaturation type 2A4 is a rare disease[1].
Key Facts
- amelogenesis imperfecta hypomaturation type 2A4's instance of is recorded as rare disease[2].
- amelogenesis imperfecta hypomaturation type 2A4's instance of is recorded as class of disease[3].
- amelogenesis imperfecta hypomaturation type 2A4's subclass of is recorded as amelogenesis imperfecta[4].
- amelogenesis imperfecta hypomaturation type 2A4's subclass of is recorded as autosomal recessive disease[5].
- amelogenesis imperfecta hypomaturation type 2A4's OMIM ID is recorded as 614832[6].
- amelogenesis imperfecta hypomaturation type 2A4's Disease Ontology ID is recorded as DOID:0110062[7].
- amelogenesis imperfecta hypomaturation type 2A4's health specialty is recorded as gastroenterology[8].
- amelogenesis imperfecta hypomaturation type 2A4's genetic association is recorded as ODAPH[9].
- amelogenesis imperfecta hypomaturation type 2A4's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110062[10].
- amelogenesis imperfecta hypomaturation type 2A4's exact match is recorded as http://identifiers.org/doid/DOID:0110062[11].
- amelogenesis imperfecta hypomaturation type 2A4's UMLS CUI is recorded as C3553830[12].
- amelogenesis imperfecta hypomaturation type 2A4's ICD-10-CM is recorded as K00.5[13].
- amelogenesis imperfecta hypomaturation type 2A4's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- amelogenesis imperfecta hypomaturation type 2A4's Mondo ID is recorded as MONDO_0013906[15].
- amelogenesis imperfecta hypomaturation type 2A4's UniProt disease ID is recorded as DI-03537[16].