All terms in MONDO
| Label |
Id |
Description |
|
mitochondrial complex 1 deficiency, nuclear type 12
|
MONDO_0026720 |
|
|
central nervous system chondroma
|
MONDO_0002779 |
|
|
intraventricular meningioma
|
MONDO_0002772 |
|
|
obsolete diarrhea, congenital
|
MONDO_0000117 |
|
|
obsolete cortical dysplasia, complex, with other brain malformations
|
MONDO_0000116 |
|
|
obsolete MONDO:0002773
|
MONDO_0002773 |
|
|
nephrotic syndrome, type 20
|
MONDO_0026726 |
|
|
intellectual developmental disorder, X-linked 108
|
MONDO_0026723 |
|
|
non-syndromic X-linked intellectual disability
|
MONDO_0019181 |
|
|
obsolete chordoid glioma
|
MONDO_0002774 |
|
|
anovulation
|
MONDO_0002775 |
|
|
Paganini-Miozzo syndrome
|
MONDO_0026724 |
|
|
tooth agenesis, selective, 7
|
MONDO_0014749 |
|
|
progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome
|
MONDO_0014748 |
|
|
glaucoma 1, open angle, K
|
MONDO_0012102 |
|
|
woolly hair, autosomal recessive 3
|
MONDO_0014765 |
|
|
spastic paraplegia-severe developmental delay-epilepsy syndrome
|
MONDO_0014764 |
|
|
spinocerebellar ataxia type 25
|
MONDO_0012103 |
|
|
obsolete Bombay phenotype
|
MONDO_0014763 |
|
|
major depressive disorder 2
|
MONDO_0012100 |
|
