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All terms in MONDO

Label Id Description
Joubert syndrome 23 MONDO_0014664
mandibulofacial dysostosis with ptosis, autosomal dominant MONDO_0012001
autosomal recessive nonsyndromic hearing loss 40 MONDO_0012002
Silver-Russell syndrome 3 MONDO_0014663
scimitar anomaly, multiple cardiac malformations, and craniofacial and central nervous system abnormalities MONDO_0012007
Lelis syndrome MONDO_0012008
cone-rod dystrophy 21 MONDO_0014669
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4 MONDO_0014668
growth failure, microcephaly, intellectual disability, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy MONDO_0012005
craniosynostosis with ocular abnormalities and hallucal defects MONDO_0012006
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3 MONDO_0014667
obsolete ectodermal dysplasia MONDO_0000019
congenital insensitivity to pain-hypohidrosis syndrome MONDO_0014662
specific phobia MONDO_0012000
phobic disorder MONDO_0003699
epidermolysis bullosa simplex with nail dystrophy MONDO_0014661
microcephaly 15, primary, autosomal recessive MONDO_0014660
obsolete familial cold autoinflammatory syndrome MONDO_0000025
obsolete exostoses, multiple MONDO_0000024
obsolete pseudomyxoma peritonei MONDO_0002689