|
1
|
(HPO:0000108)
|
Renal corticomedullary cysts |
|
|
|
|
21 / 7739
|
|
2
|
(HPO:0000238)
|
Hydrocephalus |
|
|
|
|
278 / 7739
|
|
3
|
(HPO:0001561)
|
Polyhydramnios |
|
|
|
|
191 / 7739
|
|
4
|
(HPO:0002119)
|
Ventriculomegaly |
|
|
|
|
253 / 7739
|
|
5
|
(OMIM)
|
Echodense kidneys on ultrasound |
|
|
|
|
1 / 7739
|
|
6
|
(OMIM)
|
Cystic tubular dilatation in the corticomedullary area and medulla |
|
|
|
|
1 / 7739
|
|
7
|
(OMIM)
|
Cysts contain eosinophilic proteinaceous material |
|
|
|
|
1 / 7739
|
|
8
|
(HPO:0001162)
|
Postaxial hand polydactyly |
|
|
|
|
119 / 7739
|
|
9
|
(HPO:0100259)
|
Postaxial polydactyly |
|
|
|
|
85 / 7739
|
|
10
|
(OMIM)
|
Focal hyperplasia of the choroid plexus |
|
|
|
|
1 / 7739
|
|
11
|
(OMIM)
|
Increased amniotic fluid |
|
|
|
|
1 / 7739
|
|
12
|
(OMIM)
|
Increased alpha-fetoprotein in amniotic fluid |
|
|
|
|
1 / 7739
|
|
13
|
(OMIM)
|
Increased acetylcholinesterase (AChE) in amniotic fluid |
|
|
|
|
1 / 7739
|
|
14
|
(HPO:0000007)
|
Autosomal recessive inheritance |
|
|
|
|
2538 / 7739
|
|
15
|
(HPO:0000083)
|
Renal insufficiency |
|
|
|
|
232 / 7739
|
|
16
|
(HPO:0001250)
|
Seizures |
|
|
|
|
1245 / 7739
|
|
17
|
(HPO:0001622)
|
Premature birth |
rare [HPO:skoehler]
|
|
|
|
100 / 7739
|
|
18
|
(HPO:0001629)
|
Ventricular septal defect |
rare [HPO:skoehler]
|
|
|
|
316 / 7739
|