All terms in MONDO
| Label |
Id |
Description |
|
obsolete secondary interstitial lung disease specific to childhood associated with a metabolic disease
|
MONDO_0017024 |
|
|
pontocerebellar hypoplasia, type 12
|
MONDO_0032643 |
|
|
obsolete type 11 collagen-related bone disorder
|
MONDO_0019687 |
|
|
epidermodysplasia verruciformis, susceptibility to, 3
|
MONDO_0032644 |
|
|
obsolete type 2 collagen-related bone disorder
|
MONDO_0019686 |
|
|
mirror movements 4
|
MONDO_0032641 |
|
|
arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development
|
MONDO_0032642 |
|
|
obsolete secondary interstitial lung disease specific to childhood associated with a systemic disease
|
MONDO_0017020 |
|
|
obsolete syndactyly type 2
|
MONDO_0019683 |
|
|
congenital sialidosis type 2
|
MONDO_0019682 |
|
|
sialidosis type 2
|
MONDO_0009738 |
|
|
obsolete secondary interstitial lung disease specific to childhood associated with a connective tissue disease
|
MONDO_0017021 |
|
|
obsolete secondary interstitial lung disease specific to childhood associated with a systemic vasculitis
|
MONDO_0017022 |
|
|
obsolete secondary interstitial lung disease specific to childhood associated with a granulomatous disease
|
MONDO_0017023 |
|
|
obsolete rare bone disease
|
MONDO_0019684 |
|
|
juvenile sialidosis type 2
|
MONDO_0019681 |
|
|
hearing loss, autosomal recessive 112
|
MONDO_0032639 |
|
|
genochondromatosis type 2
|
MONDO_0019680 |
|
|
mitochondrial complex 1 deficiency, nuclear type 33
|
MONDO_0032636 |
|
|
ciliary dyskinesia, primary, 39
|
MONDO_0032637 |
|
