Branchial cyst

Symptom Information:

Symptom ID: HPO:0009796
Branchial cleft cyst [HPO:0009796]
Branchial cleft cyst [Orphanet:13520]
Branchial cleft cyst (disorder) [Orphanet:13520]
Branchioma (morphologic abnormality) [Orphanet:13520]
Branchioma [Orphanet:13520]
Branchial/posterior auricular/preauricular/cheek cysts/fistulae [Orphanet:13520]
Branchial cyst [Orphanet:13520]
Branchial cyst [MedDRA:10006164]
Branchial cleft cyst [MedDRA:10006164]
Branchial cleft cysts [OMIM:Branchial cleft cysts]
Branchial cleft cyst [MedDRA:10006160]
Postauricular branchial cleft cyst [Orphanet:13520]
Postauricular fistula [MedDRA:10036329]
Postauricular branchial cleft fistula [Orphanet:13520]
Postauricular fistula (disorder) [Orphanet:13520]
Postauricular fistula [Orphanet:13520]
Preauricular cyst [MedDRA:10036509]
Preauricular branchial cleft cyst [Orphanet:13520]
Preauricular cyst (disorder) [Orphanet:13520]
Preauricular cyst [Orphanet:13520]
Cross references:
HPO:0100272 "Branchial sinus" [Orphanet:13520]
HPO:0009795 "Branchial fistula" [Orphanet:13520]
Orphanet:13520 "Branchial/posterior auricular/preauricular/cheek cysts/fistulae" [Orphanet:13520]
OMIM: "Branchial cleft cysts" [OMIM:Branchial cleft cysts]
UMLS:C0006131 "Branchioma" [Orphanet:13520]
UMLS:C0395905 "Postauricular fistula" [Orphanet:13520]
UMLS:C0158599 "Preauricular cyst" [Orphanet:13520]
Is a (Direct Parents):
Orphanet Preauricular pit
MedDRA Pharyngeal and laryngeal neoplasms benign
HPO         Branchial anomaly
Orphanet Branchial anomaly
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)
                Branchial cyst(HPO:0009796)
Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104)
    Respiratory and mediastinal neoplasms benign (excl mesotheliomas)(MedDRA:10038667)
       Pharyngeal and laryngeal neoplasms benign(MedDRA:10034807)
          Branchial cyst(HPO:0009796)
Database Frequency: 32 / 7739

All diseases associated with this symptom:

8p11.2 deletion syndrome (Orphanet:251066)
Acro-oto-ocular syndrome (Orphanet:2980)
Acrocraniofacial dysostosis (Orphanet:949)
Acrofacial dysostosis, Catania type (Orphanet:1786)
Auriculoocular anomalies - cleft lip (Orphanet:71270)
BOR syndrome (Orphanet:107)
Beckwith-Wiedemann syndrome (Orphanet:116)
Blepharophimosis-intellectual deficit syndrome, SBBYS type (Orphanet:3047)
Branchio-oculo-facial syndrome (Orphanet:1297)
Branchio-otic syndrome (Orphanet:52429)
Branchiogenic deafness syndrome (Orphanet:50815)
Cat-eye syndrome (Orphanet:195)
Conductive deafness - malformed external ear (Orphanet:3216)
Deafness - ear malformation - facial palsy (Orphanet:3232)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Distal 22q11.2 microduplication syndrome (Orphanet:261337)
Distal monosomy 3p (Orphanet:1620)
Distal trisomy 15q (Orphanet:1707)
GMS syndrome (Orphanet:2090)
Gonadal dysgenesis, XY type - associated anomalies (Orphanet:1770)
Hypertelorism, Teebi type (Orphanet:1519)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Lambert syndrome (Orphanet:1296)
Microcephaly - cardiac defect - lung malsegmentation (Orphanet:2516)
Oculoauriculovertebral spectrum with radial defects (Orphanet:2549)
Otofaciocervical syndrome (Orphanet:2792)
Spondylo-ocular syndrome (Orphanet:85194)
Tetralogy of Fallot (Orphanet:3303)
Treacher-Collins syndrome (Orphanet:861)
Trisomy 13 (Orphanet:3378)
Weaver-Williams syndrome (Orphanet:3448)