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All terms in MONDO

Label Id Description
multiple cutaneous and mucosal venous malformations MONDO_0010842
Waardenburg syndrome type 2B MONDO_0010841
congenital cardiovascular shunt MONDO_0022822
congenital contractures MONDO_0022823
congenital craniosynostosis maternal hyperthyroiditis MONDO_0022824
congenital cystic eye MONDO_0022825
congenital cystic eye multiple ocular and intracranial anomalies MONDO_0022826
PHAVER syndrome MONDO_0009859
Pfeiffer-Palm-Teller syndrome MONDO_0009858
persistent Mullerian duct syndrome MONDO_0009857
pseudohermaphroditism MONDO_0005518
congenital heart disease ptosis hypodontia craniostosis MONDO_0022831
Peters plus syndrome MONDO_0009856
congenital heart disease radio ulnar synostosis intellectual disability MONDO_0022832
Hirschsprung disease, susceptibility to, 2 MONDO_0010833
d-bifunctional protein deficiency MONDO_0009855
Bardet-Biedl syndrome 3 MONDO_0010832
peroneus tertius muscle, absence of MONDO_0009854
pterygium colli-intellectual disability-digital anomalies syndrome MONDO_0010835
Hirschsprung disease, susceptibility to, 5 MONDO_0010834