|
1
|
(HPO:0010628)
|
Facial palsy |
Very frequent [Orphanet]
|
|
|
|
146 / 7739
|
|
2
|
(HPO:0009796)
|
Branchial cyst |
Frequent [Orphanet]
|
|
|
|
32 / 7739
|
|
3
|
(HPO:0004452)
|
Abnormality of the middle ear ossicles |
Very frequent [Orphanet]
|
|
|
|
26 / 7739
|
|
4
|
(HPO:0009738)
|
Abnormality of the antihelix |
Very frequent [Orphanet]
|
|
|
|
37 / 7739
|
|
5
|
(HPO:0000405)
|
Conductive hearing impairment |
Very frequent [Orphanet]
|
|
|
|
164 / 7739
|
|
6
|
(HPO:0007209)
|
Facial paralysis |
|
|
|
|
8 / 7739
|
|
7
|
(HPO:0008572)
|
External ear malformation |
|
|
|
|
6 / 7739
|
|
8
|
(HPO:0008628)
|
Abnormality of the stapes |
|
|
|
|
1 / 7739
|
|
9
|
(HPO:0009906)
|
Aplasia/Hypoplasia of the earlobes |
Very frequent [Orphanet]
|
|
|
|
41 / 7739
|
|
10
|
(OMIM)
|
Variable external ear malformation |
|
|
|
|
1 / 7739
|
|
11
|
(HPO:0000372)
|
Abnormality of the auditory canal |
Very frequent [Orphanet]
|
|
|
|
49 / 7739
|
|
12
|
(HPO:0008772)
|
Aplasia/Hypoplasia of the external ear |
Very frequent [Orphanet]
|
|
|
|
67 / 7739
|
|
13
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|