Branchial anomaly

Symptom Information:

Symptom ID: HPO:0009794
Branchial anomalies [HPO:0009794]
Branchial arch anomaly [Orphanet:13500]
Branchial cleft anomaly (disorder) [Orphanet:13500]
Branchial cleft (disorder) [Orphanet:13500]
Branchial Clefts-Congenital disorder [Orphanet:13500]
Branchial anomalies [OMIM:Branchial anomalies]
Branchial archs anomalies [Orphanet:13500]
Branchial arch anomaly [OMIM:Branchial arch anomaly]
Cross references:
Orphanet:13500 "Branchial archs anomalies" [Orphanet:13500]
OMIM: "Branchial anomalies" [OMIM:Branchial anomalies]
OMIM: "Branchial arch anomaly" [OMIM:Branchial arch anomaly]
UMLS:C0079037 "Branchial Clefts-Congenital disorder" [Orphanet:13500]
Is a (Direct Parents):
Orphanet Hearing abnormality
HPO         Abnormality of the neck
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the neck(HPO:0000464)
             Branchial anomaly(HPO:0009794)
Database Frequency: 5 / 7739

All diseases associated with this symptom:

Branchio-oculo-facial syndrome (Orphanet:1297)
Goldenhar syndrome (Orphanet:374)
Holoprosencephaly (Orphanet:2162)
Hypomandibular faciocranial dysostosis (Orphanet:1790)
X-linked mandibulofacial dysostosis (Orphanet:1131)