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All terms in MONDO

Label Id Description
obsolete endosteal sclerosis-cerebellar hypoplasia syndrome MONDO_0008940
aplasia cutis autosomal recessive MONDO_0021907
aplasia cutis congenita MONDO_0007145
aplasia cutis congenita dominant MONDO_0021908
obsolete aplasia cutis congenita recessive MONDO_0021909
aortopulmonary window MONDO_0021902
apert-like polydactyly syndrome MONDO_0021905
CHAND syndrome MONDO_0008959
Klippel-Feil syndrome 2, autosomal recessive MONDO_0008958
isolated Klippel-Feil syndrome MONDO_0016520
dysostosis with predominant vertebral with and without costal involvement MONDO_0800075
cervical vertebrae, agenesis of MONDO_0008957
obsolete congenital neuronal ceroid lipofuscinosis MONDO_0008956
cerebrooculofacioskeletal syndrome 1 MONDO_0008955
peroxisome biogenesis disorder 2A (Zellweger) MONDO_0008954
peroxisome biogenesis disorder due to PEX5 defect MONDO_0100262
classic presentation MONDO_0100356
peroxisome biogenesis disorder 1A (Zellweger) MONDO_0008953
peroxisome biogenesis disorder due to PEX1 defect MONDO_0100259
obsolete cerebrofaciothoracic dysplasia MONDO_0008952