|
myopia, high, with cataract and vitreoretinal degeneration
|
13670 |
|
|
myopia, high, with cataract and vitreoretinal degeneration; MCVD
|
http://purl.obolibrary.org/obo/MONDO_0013670 |
|
|
cone dystrophy with night blindness and supernormal rod responses, KCNV2-Related
|
C563678 |
|
|
epilepsy, familial, with nocturnal wandering and ictal fear
|
C563679 |
|
|
endosteal hyperostosis worth type
|
C536748 |
|
|
autosomal dominant worth type with torus palatinus osteosclerosis
|
C536748 |
|
|
trisomy xq25 x chromosome
|
C536733 |
|
|
monosomy xq28 x chromosome
|
C536755 |
|
|
immunoneurologic disorder, x-linked
|
C536743 |
|
|
anemia, sideroblastic, x-linked
|
C536761 |
|
