|
1
|
(HPO:0000684)
|
Delayed eruption of teeth |
Very frequent [Orphanet]
|
|
|
|
117 / 7739
|
|
2
|
(HPO:0000708)
|
Behavioral abnormality |
Frequent [Orphanet]
|
|
|
|
212 / 7739
|
|
3
|
(HPO:0007759)
|
Opacification of the corneal stroma |
|
|
|
|
77 / 7739
|
|
4
|
(HPO:0007957)
|
Corneal opacity |
|
|
|
|
84 / 7739
|
|
5
|
(HPO:0000680)
|
Delayed eruption of primary teeth |
|
|
|
|
10 / 7739
|
|
6
|
(HPO:0001131)
|
Corneal dystrophy |
|
|
|
|
56 / 7739
|
|
7
|
(HPO:0006352)
|
Failure of eruption of permanent teeth |
|
|
|
|
2 / 7739
|
|
8
|
(HPO:0009804)
|
Reduced number of teeth |
Very frequent [Orphanet]
|
|
|
|
137 / 7739
|
|
9
|
(OMIM)
|
Failure of secondary teeth eruption |
|
|
|
|
1 / 7739
|
|
10
|
(HPO:0000168)
|
Abnormality of the gingiva |
Very frequent [Orphanet]
|
|
|
|
51 / 7739
|
|
11
|
(HPO:0000481)
|
Abnormality of the cornea |
Very frequent [Orphanet]
|
|
|
|
124 / 7739
|
|
12
|
(HPO:0000164)
|
Abnormality of the teeth |
Frequent [Orphanet]
|
|
|
|
291 / 7739
|
|
13
|
(HPO:0012758)
|
Neurodevelopmental delay |
Frequent [Orphanet]
|
|
|
|
949 / 7739
|
|
14
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|