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All terms in MONDO

Label Id Description
dandy-walker malformation with occipital cephalocele, autosomal dominant MONDO_0012218
spondyloepiphyseal dysplasia tarda, autosomal recessive, Leroy-Spranger type MONDO_0012219
Keshan disease MONDO_0000241
coxsackievirus infectious disease MONDO_0005721
invasive aspergillosis MONDO_0000240
pulmonary aspergilloma MONDO_0000266
obsolete LFS3 MONDO_0012234
obsolete portal hypertension, noncirrhotic MONDO_0014897
congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome MONDO_0014896
autosomal recessive spinocerebellar ataxia 7 MONDO_0012235
developmental and epileptic encephalopathy, 40 MONDO_0014895
stuttering, familial persistent, 2 MONDO_0012232
Li-Fraumeni syndrome 2 MONDO_0012233
Meier-Gorlin syndrome 7 MONDO_0014894
Meier-Gorlin syndrome MONDO_0016817
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2 MONDO_0012238
autosomal dominant progressive external ophthalmoplegia MONDO_0008003
congenital myopathy 4B, autosomal recessive MONDO_0012239
intermediate nemaline myopathy MONDO_0015736
childhood-onset nemaline myopathy MONDO_0015738