All terms in MONDO
| Label |
Id |
Description |
|
spondylometaphyseal dysplasia, Golden type
|
MONDO_0010738 |
|
|
neuropathy, painful
|
MONDO_0009752 |
|
|
spondyloepiphyseal dysplasia tarda, X-linked
|
MONDO_0010737 |
|
|
neuropathy, hereditary sensory, atypical
|
MONDO_0009751 |
|
|
neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive
|
MONDO_0009750 |
|
|
Taqi polymorphism
|
MONDO_0010739 |
|
|
ulnar hypoplasia-split foot syndrome
|
MONDO_0010750 |
|
|
VACTERL association, X-linked, with or without hydrocephalus
|
MONDO_0010752 |
|
|
unique green phenomenon
|
MONDO_0010751 |
|
|
van den Bosch syndrome
|
MONDO_0010754 |
|
|
cardiac valvular dysplasia, X-linked
|
MONDO_0010753 |
|
|
oculo digital syndrome
|
MONDO_0022712 |
|
|
chester porphyria
|
MONDO_0022714 |
|
|
Chiari malformation type 3
|
MONDO_0022715 |
|
|
Chiari malformation type 4
|
MONDO_0022716 |
|
|
congenital dyserythropoietic anemia type 3
|
MONDO_0007109 |
|
|
oculo-palato-cerebral syndrome
|
MONDO_0009769 |
|
|
anal sphincter dysplasia
|
MONDO_0007106 |
|
|
anal sphincter myopathy, internal
|
MONDO_0007107 |
|
|
oculodentodigital dysplasia, autosomal recessive
|
MONDO_0009768 |
|
