|
cone-ROD dystrophy 16; CORD16
|
http://purl.obolibrary.org/obo/MONDO_0013786 |
|
|
teratoma, benign (morphologic abnormality)
|
2378 |
|
|
rhabdomyosarcoma embryonal 1
|
C537883 |
|
|
lattice type 1 CDL1 corneal dystrophy
|
C537881 |
|
|
distal, type 1 arthrogryposis
|
C535378 |
|
|
distal type 1 arthrogryposis multiplex congenita
|
C535378 |
|
|
monosomy 8p23 1 chromosome 8
|
C537827 |
|
|
lattice type 1 corneal dystrophy
|
C537881 |
|
|
polymicrogyria-turricephaly-hypogenitalism syndrome
|
http://purl.obolibrary.org/obo/MONDO_0017378 |
|
|
partial deletion (short arm) chromosome 8
|
C537826 |
|
|
deficiency of 3-beta-hydroxysteroid-delta(5)-desaturase
|
C537880 |
|
