| C1848488 |
Pierre Robin syndrome with fetal chondrodysplasia |
DO |
Stickler syndrome
|
0080046 |
| C1848488 |
Pierre Robin syndrome with fetal chondrodysplasia |
MONDO |
Stickler syndrome type 3
|
0008490 |
| C1848488 |
Pierre Robin syndrome with fetal chondrodysplasia |
MONDO |
otospondylomegaepiphyseal dysplasia
|
0008975 |
| C1848488 |
Pierre Robin syndrome with fetal chondrodysplasia |
MONDO |
Weissenbacher-Zweymuller syndrome
|
0010195 |
| C1848488 |
Pierre Robin syndrome with fetal chondrodysplasia |
MONDO |
Stickler syndrome
|
0019354 |
| C1848488 |
Pierre Robin syndrome with fetal chondrodysplasia |
MSH |
Pierre Robin syndrome with fetal chondrodysplasia
|
C535776 |
| C1848488 |
Pierre Robin syndrome with fetal chondrodysplasia |
OMIM |
OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT
|
184840 |
| C1848488 |
Pierre Robin syndrome with fetal chondrodysplasia |
OMIM |
OSMED, HETEROZYGOUS
|
184840 |
| C1848488 |
Pierre Robin syndrome with fetal chondrodysplasia |
ORDO |
Autosomal dominant otospondylomegaepiphyseal dysplasia
|
166100 |
| C1848488 |
Pierre Robin syndrome with fetal chondrodysplasia |
ORDO |
Weissenbacher- Zweymuller syndrome
|
3450 |