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- B4fc090d6353b27a48d3b04bf65116acc hasDbXref "Orphanet:83463" @default.
- B4fc090d6353b27a48d3b04bf65116acc hasDbXref "https://orcid.org/0000-0001-5208-3432" @default.
- B4fc090d6353b27a48d3b04bf65116acc type Axiom @default.
- B4fc090d6353b27a48d3b04bf65116acc annotatedProperty IAO_0000115 @default.
- B4fc090d6353b27a48d3b04bf65116acc annotatedSource MONDO_0010920 @default.
- B4fc090d6353b27a48d3b04bf65116acc annotatedTarget "A congenital malformation of the external ear, seen more frequently in males, that occurs sporadically or is inherited, that is characterized by unilateral (79-93% of cases, 60% of which involve the right ear) or bilateral small and abnormally shaped auricles and that is often associated with atresia or stenosis of the ear canal, attention deficit disorders and delayed language development. The variation in auricle size ranges from grade I, where the auricle is simply smaller than normal, to grade IV, also known as anotia, where there is a complete absence of the external ear and of the auditory canal." @default.