amelogenesis imperfecta, type IJ; AI1J
human disease
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amelogenesis imperfecta, type IJ; AI1J
Summary
amelogenesis imperfecta, type IJ; AI1J is a rare disease[1].
Key Facts
- amelogenesis imperfecta, type IJ; AI1J's instance of is recorded as rare disease[2].
- amelogenesis imperfecta, type IJ; AI1J's instance of is recorded as disease[3].
- amelogenesis imperfecta, type IJ; AI1J's instance of is recorded as class of disease[4].
- amelogenesis imperfecta, type IJ; AI1J's subclass of is recorded as genetic disease[5].
- amelogenesis imperfecta, type IJ; AI1J's subclass of is recorded as amelogenesis imperfecta[6].
- amelogenesis imperfecta, type IJ; AI1J's subclass of is recorded as autosomal recessive disease[7].
- amelogenesis imperfecta, type IJ; AI1J's OMIM ID is recorded as 617297[8].
- amelogenesis imperfecta, type IJ; AI1J's Disease Ontology ID is recorded as DOID:0080953[9].
- amelogenesis imperfecta, type IJ; AI1J's genetic association is recorded as ACP4[10].
- amelogenesis imperfecta, type IJ; AI1J's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080953[11].
- amelogenesis imperfecta, type IJ; AI1J's exact match is recorded as http://identifiers.org/doid/DOID:0080953[12].
- amelogenesis imperfecta, type IJ; AI1J's UMLS CUI is recorded as C4310630[13].
- amelogenesis imperfecta, type IJ; AI1J's Mondo ID is recorded as MONDO_0015008[14].
- amelogenesis imperfecta, type IJ; AI1J's UniProt disease ID is recorded as DI-04931[15].
- amelogenesis imperfecta, type IJ; AI1J's Experimental Factor Ontology ID is recorded as 0009302[16].