hypomaturation amelogenesis imperfecta
human disease
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hypomaturation amelogenesis imperfecta
Summary
hypomaturation amelogenesis imperfecta is a class of disease[1].
Key Facts
- hypomaturation amelogenesis imperfecta's instance of is recorded as class of disease[2].
- hypomaturation amelogenesis imperfecta's subclass of is recorded as amelogenesis imperfecta[3].
- hypomaturation amelogenesis imperfecta's MeSH descriptor ID is recorded as C536606[4].
- hypomaturation amelogenesis imperfecta's Orphanet ID is recorded as 100033[5].
- hypomaturation amelogenesis imperfecta's ICD-9-CM is recorded as 520.5[6].
- hypomaturation amelogenesis imperfecta's genetic association is recorded as AMELX[7].
- hypomaturation amelogenesis imperfecta's genetic association is recorded as MMP20[8].
- hypomaturation amelogenesis imperfecta's genetic association is recorded as WDR72[9].
- hypomaturation amelogenesis imperfecta's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_100033[10].
- hypomaturation amelogenesis imperfecta's UMLS CUI is recorded as C0399372[11].
- hypomaturation amelogenesis imperfecta's ICD-10-CM is recorded as K00.5[12].
- hypomaturation amelogenesis imperfecta's GARD rare disease ID is recorded as 8349[13].
- hypomaturation amelogenesis imperfecta's Mondo ID is recorded as MONDO_0015048[14].