All terms in MONDO
| Label |
Id |
Description |
|
geleophysic dysplasia 1
|
MONDO_0009269 |
|
|
Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome
|
MONDO_0009268 |
|
|
Gaucher disease type III
|
MONDO_0009267 |
|
|
Gaucher disease type II
|
MONDO_0009266 |
|
|
Gaucher disease type I
|
MONDO_0009265 |
|
|
neonatal hemochromatosis
|
MONDO_0009275 |
|
|
ghosal hematodiaphyseal dysplasia
|
MONDO_0009274 |
|
|
hydatidiform mole, recurrent, 1
|
MONDO_0009273 |
|
|
intellectual disability, X-linked 58
|
MONDO_0010266 |
|
|
German syndrome
|
MONDO_0009272 |
|
|
Simpson-Golabi-Behmel syndrome type 2
|
MONDO_0010265 |
|
|
Simpson-Golabi-Behmel syndrome
|
MONDO_0010731 |
|
|
geroderma osteodysplastica
|
MONDO_0009271 |
|
|
X-linked lissencephaly with abnormal genitalia
|
MONDO_0010268 |
|
|
genito-palato-cardiac syndrome
|
MONDO_0009270 |
|
|
episodic muscle weakness, X-linked
|
MONDO_0010267 |
|
|
Coats disease
|
MONDO_0010269 |
|
|
secondary dysgenetic glaucoma
|
MONDO_0020216 |
|
|
arthrogryposis, congenital, lower limb, X-linked
|
MONDO_0010260 |
|
|
hypotonia, congenital nystagmus, ataxia, and abnormal auditory brainstem responses
|
MONDO_0010262 |
|
