All terms in MONDO
| Label |
Id |
Description |
|
hearing loss, autosomal recessive 114
|
MONDO_0032761 |
|
|
obsolete hemorrhagic disorder due to a qualitative platelet defect
|
MONDO_0017142 |
|
|
lymphatic malformation 13
|
MONDO_0859379 |
|
|
obsolete genetic infertility
|
MONDO_0017143 |
|
|
hearing loss, autosomal recessive 120
|
MONDO_0859374 |
|
|
developmental delay with hypotonia, myopathy, and brain abnormalities
|
MONDO_0859375 |
|
|
intellectual developmental disorder with short stature and variable skeletal anomalies
|
MONDO_0032759 |
|
|
hydrocephalus, congenital, 5, susceptibility to
|
MONDO_0859376 |
|
|
neurodevelopmental disorder with poor growth and behavioral abnormalities
|
MONDO_0859377 |
|
|
ciliary dyskinesia, primary, 41
|
MONDO_0032757 |
|
|
neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia
|
MONDO_0032758 |
|
|
rhabdomyolysis, susceptibility to, 1
|
MONDO_0859371 |
|
|
neurodevelopmental disorder with or without variable brain abnormalities; NEDBA
|
MONDO_0032755 |
|
|
cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies
|
MONDO_0859372 |
|
|
long qt syndrome 8
|
MONDO_0032756 |
|
|
intellectual developmental disorder, autosomal recessive 78
|
MONDO_0859373 |
|
|
obsolete short sleep, familial natural, 2
|
MONDO_0020786 |
|
|
capillary malformation-arteriovenous malformation 2
|
MONDO_0020785 |
|
|
osteoma
|
MONDO_0005166 |
|
|
obsolete short sleep, familial natural, 1
|
MONDO_0020784 |
|
