|
syndrome, laurence-moon-biedl
|
D007849 |
|
|
KERATOENDOTHELIITIS fugax hereditaria
|
7849 |
|
|
laurence moon biedl syndrome
|
D007849 |
|
|
growth retardation, cataract, hearing loss, and unusual appearance microcephaly
|
C567849 |
|
|
Keratoendotheliitis fugax hereditaria
|
7849 |
|
|
keratitis fugax hereditaria
|
7849 |
|
|
KERATOENDOTHELIITIS fugax hereditaria; KEFH
|
http://purl.obolibrary.org/obo/MONDO_0007849 |
|
|
fatal multisystem syndrome involving the eyes, ears, lungs, intestines, and kidneys
|
17849 |
|
|
congenital progressive oculo-acoustico-cerebral degeneration
|
C537849 |
|
