Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Entire branchial arch |
Is a |
True |
Branchial arch structure |
Inferred relationship |
Some |
|
Fifth branchial arch structure (body structure) |
Is a |
True |
Branchial arch structure |
Inferred relationship |
Some |
|
Sixth branchial arch structure |
Is a |
True |
Branchial arch structure |
Inferred relationship |
Some |
|
First branchial arch structure |
Is a |
True |
Branchial arch structure |
Inferred relationship |
Some |
|
Second branchial arch structure |
Is a |
True |
Branchial arch structure |
Inferred relationship |
Some |
|
Fourth branchial arch structure (body structure) |
Is a |
True |
Branchial arch structure |
Inferred relationship |
Some |
|
Third branchial arch structure |
Is a |
True |
Branchial arch structure |
Inferred relationship |
Some |
|
Excision of branchial cyst |
Procedure site |
False |
Branchial arch structure |
Inferred relationship |
Some |
|
Excision of branchial fistula |
Procedure site |
False |
Branchial arch structure |
Inferred relationship |
Some |
2 |
Primary malignant neoplasm of branchial cleft |
Finding site |
False |
Branchial arch structure |
Inferred relationship |
Some |
|
Excision of branchial tract |
Procedure site |
False |
Branchial arch structure |
Inferred relationship |
Some |
2 |
Excision of branchial sinus |
Procedure site |
False |
Branchial arch structure |
Inferred relationship |
Some |
3 |
Cervical auricle |
Finding site |
False |
Branchial arch structure |
Inferred relationship |
Some |
2 |
Branchial cleft cyst |
Finding site |
False |
Branchial arch structure |
Inferred relationship |
Some |
1 |
Repair of branchial cleft fistula or cyst |
Procedure site |
False |
Branchial arch structure |
Inferred relationship |
Some |
|
Excision of branchial cleft vestige |
Procedure site |
False |
Branchial arch structure |
Inferred relationship |
Some |
|
Brachial cleft vestige excised |
Procedure site |
False |
Branchial arch structure |
Inferred relationship |
Some |
4 |
Developmental malformation of branchial arch (disorder) |
Finding site |
False |
Branchial arch structure |
Inferred relationship |
Some |
1 |
Midline cervical cleft (disorder) |
Finding site |
False |
Branchial arch structure |
Inferred relationship |
Some |
2 |
Branchial cleft cyst |
Finding site |
False |
Branchial arch structure |
Inferred relationship |
Some |
1 |
Cervical auricle |
Finding site |
False |
Branchial arch structure |
Inferred relationship |
Some |
2 |
Midline cervical cleft (disorder) |
Finding site |
False |
Branchial arch structure |
Inferred relationship |
Some |
2 |
Developmental malformation of branchial arch (disorder) |
Finding site |
True |
Branchial arch structure |
Inferred relationship |
Some |
1 |
Developmental malformation of branchial arch (disorder) |
Finding site |
False |
Branchial arch structure |
Inferred relationship |
Some |
3 |
Midline cervical cleft (disorder) |
Finding site |
False |
Branchial arch structure |
Inferred relationship |
Some |
6 |
Fourth branchial cleft cyst (disorder) |
Finding site |
False |
Branchial arch structure |
Inferred relationship |
Some |
2 |
First branchial cleft cyst |
Finding site |
False |
Branchial arch structure |
Inferred relationship |
Some |
2 |
Second branchial cleft cyst |
Finding site |
False |
Branchial arch structure |
Inferred relationship |
Some |
2 |
Third branchial cleft cyst (disorder) |
Finding site |
False |
Branchial arch structure |
Inferred relationship |
Some |
2 |
A very rare syndrome described in four siblings of one French family and characterized by branchial dysplasia (malar hypoplasia, macrostomia, preauricular tags and meatal atresia), club feet, inguinal herniae and cholestasis due to paucity of interlobular bile ducts and intellectual deficit. |
Finding site |
True |
Branchial arch structure |
Inferred relationship |
Some |
1 |
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). |
Finding site |
True |
Branchial arch structure |
Inferred relationship |
Some |
2 |
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). |
Finding site |
False |
Branchial arch structure |
Inferred relationship |
Some |
1 |
Melnick-Fraser syndrome |
Finding site |
True |
Branchial arch structure |
Inferred relationship |
Some |
5 |
Epibulbar lipodermoid - preauricular appendages - polythelia is a branchial arch syndrome described in seven sibs of one Danish family and characterized by supernumerary nipples (polythelia), preauricular appendages and often binocular epibulbar lipodermoids or unilateral subconjunctival lipodermoids. |
Finding site |
True |
Branchial arch structure |
Inferred relationship |
Some |
2 |
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by choanal atresia, athelia or hypoplastic nipples, branchial arch abnormalities, external ear malformations, hearing loss, thyroid abnormalities, delayed or absent pubertal development, and short stature. Developmental delay/intellectual disability are variably reported. |
Finding site |
True |
Branchial arch structure |
Inferred relationship |
Some |
3 |