retinitis pigmentosa, and sutural cataract microcephaly
|
C563296 |
|
cataract, congenital, blue dot type, 2
|
C563294 |
|
prefrontal, with bone cysts dementia
|
C536329 |
|
congenital, blue dot type, 2 cataract
|
C563294 |
|
epiphyseal dysplasia, multiple, with robin phenotype
|
C563291 |
|
progressive, with lipomembranous polycystic osteodysplasia dementia
|
C536329 |
|
multiple epiphyseal dysplasia with robin phenotype
|
C563291 |
|
multiple, with robin phenotype epiphyseal dysplasia
|
C563291 |
|
paranasal sinus olfactory neuroblastoma
|
6329 |
|
syndrome associated with hypertrophic cardiomyopathy
|
http://purl.obolibrary.org/obo/MONDO_0016329 |
|
congenital, cerulean type, 2 cataract
|
C563294 |
|
ectopia lentis, spontaneous filtering blebs, and craniofacial dysmorphism
|
C563293 |
|