JSON

All terms in MONDO

Label Id Description
fundus dystrophy, pseudoinflammatory, recessive form MONDO_0009918
autosomal recessive pseudohypoaldosteronism type 1 MONDO_0009917
pseudohypoaldosteronism type 1 MONDO_0019161
46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency MONDO_0009916
46,XX disorder of sex development-skeletal anomalies syndrome MONDO_0009915
pseudodiastrophic dysplasia MONDO_0009914
prune belly syndrome with pulmonic stenosis, intellectual disability, and deafness MONDO_0009913
prolactin deficiency with obesity and enlarged testes MONDO_0009912
prolactin deficiency, isolated MONDO_0009911
Wiedemann-Rautenstrauch syndrome MONDO_0009910
peroxisomal acyl-CoA oxidase deficiency MONDO_0009919
familial hypertryptophanemia MONDO_0010907
neonatal acute respiratory distress due to SP-B deficiency MONDO_0009929
orofacial cleft 11 MONDO_0010906
pulmonary alveolar microlithiasis MONDO_0009928
UV-sensitive syndrome 1 MONDO_0010909
UV-sensitive syndrome MONDO_0015797
3MC syndrome 2 MONDO_0009927
loose anagen syndrome MONDO_0010908
autosomal recessive inherited pseudoxanthoma elasticum MONDO_0009925