All terms in MONDO
| Label |
Id |
Description |
|
six2-related frontonasal dysplasia
|
MONDO_0044628 |
|
|
autosomal dominant charcot-marie-tooth disease type 2 due to DGAT2 mutation
|
MONDO_0044625 |
|
|
pediatric collagenous gastritis
|
MONDO_0044624 |
|
|
conductive hearing loss disorder
|
MONDO_0020679 |
|
|
acute macular neuroretinopathy
|
MONDO_0044627 |
|
|
female infertility due to oocyte meiotic arrest
|
MONDO_0044626 |
|
|
intellectual developmental disorder, autosomal recessive 68
|
MONDO_0032665 |
|
|
neuroepithelioma
|
MONDO_0017046 |
|
|
epidermodysplasia verruciformis, susceptibility to, 4
|
MONDO_0032666 |
|
|
infantile axonal neuropathy
|
MONDO_0017047 |
|
|
autism, susceptibility to, 20
|
MONDO_0030004 |
|
|
pseudomyxoma peritonei
|
MONDO_0017048 |
|
|
developmental and epileptic encephalopathy, 70
|
MONDO_0032663 |
|
|
ciliary dyskinesia, primary, 40
|
MONDO_0032664 |
|
|
neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia
|
MONDO_0032661 |
|
|
intellectual developmental disorder, autosomal recessive 67
|
MONDO_0032662 |
|
|
mesoblastic nephroma
|
MONDO_0003130 |
|
|
adult familial nephronophthisis-spastic quadriparesia syndrome
|
MONDO_0017044 |
|
|
neuroectodermal-endocrine syndrome
|
MONDO_0017045 |
|
|
spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant
|
MONDO_0032660 |
|
