|
1
|
(HPO:0002667)
|
Nephroblastoma |
Occasional [Orphanet]
|
|
|
|
30 / 7739
|
|
2
|
(HPO:0001528)
|
Hemihypertrophy |
|
|
|
|
13 / 7739
|
|
3
|
(HPO:0100555)
|
Asymmetric growth |
Very frequent [Orphanet]
|
|
|
|
25 / 7739
|
|
4
|
(HPO:0011331)
|
Hemifacial atrophy |
Frequent [Orphanet]
|
|
|
|
79 / 7739
|
|
5
|
(HPO:0001315)
|
Reduced tendon reflexes |
Occasional [Orphanet]
|
|
|
|
160 / 7739
|
|
6
|
(HPO:0001555)
|
Asymmetry of the thorax |
Very frequent [Orphanet]
|
|
|
|
15 / 7739
|
|
7
|
(HPO:0007021)
|
Pain insensitivity |
Occasional [Orphanet]
|
|
|
|
35 / 7739
|
|
8
|
(HPO:0030680)
|
Abnormality of cardiovascular system morphology |
Occasional [Orphanet]
|
|
|
|
355 / 7739
|
|
9
|
(HPO:0002475)
|
Myelomeningocele |
Occasional [Orphanet]
|
|
|
|
29 / 7739
|
|
10
|
(HPO:0002650)
|
Scoliosis |
Very frequent [Orphanet]
|
|
|
|
705 / 7739
|
|
11
|
(HPO:0000164)
|
Abnormality of the teeth |
Frequent [Orphanet]
|
|
|
|
291 / 7739
|
|
12
|
(HPO:0001256)
|
Intellectual disability, mild |
20 % [HPO:skoehler]
|
|
|
|
141 / 7739
|
|
13
|
(HPO:0002898)
|
Embryonal neoplasm |
|
|
|
|
6 / 7739
|
|
14
|
(HPO:0003712)
|
Skeletal muscle hypertrophy |
|
|
|
|
42 / 7739
|
|
15
|
(HPO:0004299)
|
Hernia of the abdominal wall |
Occasional [Orphanet]
|
|
|
|
176 / 7739
|
|
16
|
(OMIM)
|
Asymmetric growth involving 1 or more body parts, isolated |
|
|
|
|
1 / 7739
|
|
17
|
(OMIM)
|
Asymmetry of the chest |
|
|
|
|
1 / 7739
|
|
18
|
(OMIM)
|
Displaced nipples due to chest asymmetry |
|
|
|
|
1 / 7739
|
|
19
|
(OMIM)
|
Increased risk of Wilms tumor |
|
|
|
|
2 / 7739
|
|
20
|
(OMIM)
|
Hemihyperplasia of limbs |
|
|
|
|
1 / 7739
|
|
21
|
(OMIM)
|
Hemihyperplasia of hands |
|
|
|
|
1 / 7739
|
|
22
|
(OMIM)
|
Hemihyperplasia of feet |
|
|
|
|
1 / 7739
|
|
23
|
(OMIM)
|
Muscle hypertrophy in affected area |
|
|
|
|
1 / 7739
|
|
24
|
(OMIM)
|
Mental retardation, mild to moderate |
|
|
|
|
33 / 7739
|
|
25
|
(OMIM)
|
Increased risk for embryonal tumors |
|
|
|
|
1 / 7739
|
|
26
|
(OMIM)
|
Increased risk for Wilms tumor |
|
|
|
|
1 / 7739
|
|
27
|
(HPO:0000079)
|
Abnormality of the urinary system |
Occasional [Orphanet]
|
|
|
|
88 / 7739
|
|
28
|
(HPO:0000035)
|
Abnormality of the testis |
Occasional [Orphanet]
|
|
|
|
296 / 7739
|
|
29
|
(HPO:0012758)
|
Neurodevelopmental delay |
Frequent [Orphanet]
|
|
|
|
949 / 7739
|
|
30
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|
|
31
|
(HPO:0003829)
|
Incomplete penetrance |
|
|
|
|
85 / 7739
|