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All terms in MONDO

Label Id Description
Fanconi anemia complementation group J MONDO_0012187
Pierson syndrome MONDO_0012184
LAMB2-related infantile-onset nephrotic syndrome MONDO_0013621
spondylometaphyseal dysplasia, A4 type MONDO_0012185
radio-digito-facial dysplasia MONDO_0024171
posterior polymorphous corneal dystrophy 2 MONDO_0012199
autosomal dominant limb-girdle muscular dystrophy type 1G MONDO_0012193
aneurysm, intracranial berry, 3 MONDO_0012194
hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 MONDO_0012191
permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome MONDO_0012192
idiopathic aplastic anemia MONDO_0012197
PCWH syndrome MONDO_0012198
arthrogryposis-severe scoliosis syndrome MONDO_0012195
autosomal dominant auditory neuropathy 1 MONDO_0012196
nephrotic syndrome - deafness - pretibial epidermolysis bullosa syndrome MONDO_0012190
portal hypertension, noncirrhotic MONDO_0024193
neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset MONDO_0024189
dry beriberi MONDO_0024182
wet beriberi MONDO_0024183
parkinsonism with polyneuropathy MONDO_0036193