All terms in MONDO
| Label |
Id |
Description |
|
vasculogenic impotence
|
MONDO_0007013 |
|
|
muscular dystrophy, adult-onset, with leukoencephalopathy
|
MONDO_0009674 |
|
|
spinal muscular atrophy, type II
|
MONDO_0009673 |
|
|
obsolete uveitis
|
MONDO_0007010 |
|
|
uveoparotid fever
|
MONDO_0007011 |
|
|
spinal muscular atrophy, type III
|
MONDO_0009672 |
|
|
muscular dystrophy, congenital, with rapid progression
|
MONDO_0009682 |
|
|
microphthalmia, syndromic 1
|
MONDO_0010671 |
|
|
Ullrich congenital muscular dystrophy 1
|
MONDO_0009681 |
|
|
Wernicke encephalopathy
|
MONDO_0007020 |
|
|
X-linked intellectual disability-spastic quadriparesis syndrome
|
MONDO_0010670 |
|
|
congenital muscular dystrophy-infantile cataract-hypogonadism syndrome
|
MONDO_0009680 |
|
|
modifier, X-linked, for Neurofunctional defects
|
MONDO_0010673 |
|
|
linear skin defects with multiple congenital anomalies
|
MONDO_0010672 |
|
|
isolated focal cortical dysplasia
|
MONDO_0019009 |
|
|
muscular dystrophy, cardiac type
|
MONDO_0010675 |
|
|
benign recurrent intrahepatic cholestasis
|
MONDO_0019008 |
|
|
familial intrahepatic cholestasis
|
MONDO_0017290 |
|
|
muscular dystrophy, Mabry type
|
MONDO_0010677 |
|
|
muscular dystrophy, Hemizygous lethal type
|
MONDO_0010676 |
|
