amelogenesis imperfecta type 1C
amelogenesis imperfecta that has material basis in homozygous mutation in the enamelin gene (ENAM)
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amelogenesis imperfecta type 1C
Summary
amelogenesis imperfecta type 1C is a rare disease[1].
Key Facts
- amelogenesis imperfecta type 1C's instance of is recorded as rare disease[2].
- amelogenesis imperfecta type 1C's instance of is recorded as class of disease[3].
- amelogenesis imperfecta type 1C's subclass of is recorded as amelogenesis imperfecta[4].
- amelogenesis imperfecta type 1C's subclass of is recorded as genetic disease[5].
- amelogenesis imperfecta type 1C's subclass of is recorded as autosomal recessive disease[6].
- amelogenesis imperfecta type 1C's OMIM ID is recorded as 204650[7].
- amelogenesis imperfecta type 1C's Disease Ontology ID is recorded as DOID:0110056[8].
- amelogenesis imperfecta type 1C's health specialty is recorded as gastroenterology[9].
- amelogenesis imperfecta type 1C's genetic association is recorded as ENAM[10].
- amelogenesis imperfecta type 1C's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110056[11].
- amelogenesis imperfecta type 1C's exact match is recorded as http://identifiers.org/doid/DOID:0110056[12].
- amelogenesis imperfecta type 1C's UMLS CUI is recorded as C2673923[13].
- amelogenesis imperfecta type 1C's ICD-10-CM is recorded as K00.5[14].
- amelogenesis imperfecta type 1C's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- amelogenesis imperfecta type 1C's Mondo ID is recorded as MONDO_0008770[16].
- amelogenesis imperfecta type 1C's UniProt disease ID is recorded as DI-00090[17].