syndromic disease hereditary disease multiple congenital anomalies/dysmorphic syndrome without intellectual disability branchiootic syndrome https://www.malacards.org/card/branchiootic_syndrome Branchiootic syndrome is a rare, genetic multiple congenital anomalies syndrome characterized by second branchial arch anomalies (branchial cysts and fistulae), malformations of the outer, middle and inner ear associated with sensorineural, mixed or conductive hearing loss, and the absence of renal abnormalities. Typical ear findings consist of malformed auricles (e.g. lop or cupped ears), preauricular pits and/or tags, and middle and/or inner ear dysplasias (including cochlear, vestibular and semicircular channel hypoplasia, malformation of the ossicles and of middle ear space). GARD:0010148 Orphanet:52429 MEDGEN:1636666 UMLS:C4273131 NANDO:1200675 SCTID:764810000 MONDO:0018878 DOID:0060232 OMIMPS:602588 MESH:C537104