Branchial cyst
Symptom Information:
Symptom ID: | HPO:0009796 | ||||||||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) 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) MedDRA: 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) |
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Database Frequency: | 32 / 7739 | ||||||||||||||||||||
Resource: |
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) |
BRANCHIOOTIC SYNDROME 3 | (OMIM:608389) |
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) |