|
1
|
(HPO:0000347)
|
Micrognathia |
|
|
|
|
426 / 7739
|
|
2
|
(HPO:0000600)
|
Abnormality of the pharynx |
Frequent [Orphanet]
|
|
|
|
22 / 7739
|
|
3
|
(HPO:0000175)
|
Cleft palate |
|
|
|
|
349 / 7739
|
|
4
|
(HPO:0002093)
|
Respiratory insufficiency |
Frequent [Orphanet]
|
|
|
|
410 / 7739
|
|
5
|
(HPO:0000162)
|
Glossoptosis |
Very frequent [Orphanet]
|
|
|
|
26 / 7739
|
|
6
|
(HPO:0000201)
|
Pierre-Robin sequence |
|
|
|
|
20 / 7739
|
|
7
|
(HPO:0001648)
|
Cor pulmonale |
|
|
|
|
16 / 7739
|
|
8
|
(HPO:0002643)
|
Neonatal respiratory distress |
|
|
|
|
22 / 7739
|
|
9
|
(HPO:0002781)
|
Upper airway obstruction |
|
|
|
|
7 / 7739
|
|
10
|
(HPO:0008872)
|
Feeding difficulties in infancy |
|
|
|
|
153 / 7739
|
|
11
|
(OMIM)
|
Neonatal feeding problems |
|
|
|
|
1 / 7739
|
|
12
|
(HPO:0000174)
|
Abnormality of the palate |
Very frequent [Orphanet]
|
|
|
|
298 / 7739
|
|
13
|
(HPO:0000277)
|
Abnormality of the mandible |
Very frequent [Orphanet]
|
|
|
|
394 / 7739
|
|
14
|
(HPO:0000007)
|
Autosomal recessive inheritance |
|
|
|
|
2538 / 7739
|