|
familial restrictive, 2 cardiomyopathy
|
C566512 |
|
|
anterior uveitis (disease)
|
6651 |
|
|
maxillary retrusion, and mental retardation scaphocephaly
|
C566511 |
|
|
congenital, with deafness, penoscrotal web, and mental retardation emphysema
|
C566519 |
|
|
maternal uniparental disomy of chromosome 1
|
16651 |
|
|
maternal uniparental disomy of chromosome type 1
|
16651 |
|
|
lethal skeletal dysplasia and progressive central nervous system degeneration
|
C566514 |
|
|
selective, 2 tooth agenesis
|
C566513 |
|
|
familial pancreatic lymphoma
|
C566516 |
|
|
cataracts, cleft palate, and mental retardation spondyloepiphyseal dysplasia with coronal craniosynostosis
|
C566515 |
|
