|
hyperekplexia, hereditary 1
|
7868 |
|
|
multisystem proteinopathy 1
|
8178 |
|
|
rhabdomyosarcoma embryonal 1
|
C537883 |
|
|
cholestasis, pregnancy-Related, 1
|
http://purl.obolibrary.org/obo/MONDO_0007829 |
|
|
lattice type 1 CDL1 corneal dystrophy
|
C537881 |
|
|
distal, type 1 arthrogryposis
|
C535378 |
|
|
distal type 1 arthrogryposis multiplex congenita
|
C535378 |
|
|
spastic quadriplegic, 1 cerebral palsy
|
C567853 |
|
|
monosomy 8p23 1 chromosome 8
|
C537827 |
|
|
fuchs endothelial, 1 corneal dystrophy
|
C535478 |
|
|
fuchs' endothelial, 1 corneal dystrophy
|
C535478 |
|
|
lattice type 1 corneal dystrophy
|
C537881 |
|
|
ebv-associated, autosomal, 1 lymphoproliferative syndrome
|
C567815 |
|
