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All terms in MONDO

Label Id Description
developmental delay with short stature, dysmorphic facial features, and sparse hair 2 MONDO_0100217
arthrogryposis multiplex congenita 5 MONDO_0100218
growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominant MONDO_0100219
Rajab interstitial lung disease with brain calcifications 2 MONDO_0100220
IFAP syndrome 2 MONDO_0100221
A20 haploinsufficiency MONDO_0100222
mitochondrial complex I deficiency, nuclear type MONDO_0100223
mitochondrial complex I deficiency MONDO_0100133
mitochondrial complex I deficiency, nuclear type 1 MONDO_0100224
isolated oxidative phosphorylation complex disorder MONDO_0016805
collagen 6-related myopathy MONDO_0100225
parasomnia, sleepwalking type MONDO_0100226
LAMA2-related muscular dystrophy MONDO_0100228
qualitative or quantitative defects of merosin MONDO_0016149
muscular dystrophy MONDO_0020121
microcephaly with intellectual disability MONDO_0100200
lumbar disc disease MONDO_0100201
vertebral column disorder MONDO_0000812
lumbar disc herniation, susceptibility to MONDO_0100202
parainfluenza virus type 1 infectious disease MONDO_0100203