All terms in MONDO
| Label |
Id |
Description |
|
Machado-Joseph disease type 3
|
MONDO_0017176 |
|
|
neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities
|
MONDO_0859347 |
|
|
hemihyperplasia-multiple lipomatosis syndrome
|
MONDO_0017177 |
|
|
PIK3CA-related overgrowth syndrome
|
MONDO_0035162 |
|
|
idiopathic recurrent stupor
|
MONDO_0017170 |
|
|
hypotrichosis 15
|
MONDO_0859341 |
|
|
mucopolysaccharidosis type 6, rapidly progressing
|
MONDO_0017171 |
|
|
microcephaly 30, primary, autosomal recessive
|
MONDO_0859342 |
|
|
mucopolysaccharidosis type 6, slowly progressing
|
MONDO_0017172 |
|
|
spinocerebellar ataxia 27B, late-onset
|
MONDO_0859340 |
|
|
obsolete peripartum cardiomyopathy
|
MONDO_0005199 |
|
|
obsolete teratozoospermia
|
MONDO_0005196 |
|
|
septic peritonitis
|
MONDO_0005195 |
|
|
adult-onset non-insulinoma persistent hyperinsulinemic hypoglycemia
|
MONDO_0017189 |
|
|
neurodevelopmental disorder with midbrain and hindbrain malformations
|
MONDO_0056797 |
|
|
spermatogenic failure 78
|
MONDO_0859338 |
|
|
tooth agenesis, selective, 10
|
MONDO_0859339 |
|
|
autosomal dominant hyperinsulinism due to Kir6.2 deficiency
|
MONDO_0017185 |
|
|
hyperinsulinemic hypoglycemia, familial, 2
|
MONDO_0011153 |
|
|
spinocerebellar ataxia 50
|
MONDO_0859334 |
|
