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All terms in MONDO

Label Id Description
congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome MONDO_0033853
genetic biliary tract disease MONDO_0015509
acrofacial dysostosis MONDO_0018237
obsolete dysostosis with limb and face anomalies as a major feature MONDO_0018236
autosomal recessive axonal charcot-marie-tooth disease due to copper metabolism defect MONDO_0033850
disorder of copper metabolism MONDO_0017762
obsolete primary bone dysplasia with progressive ossification of skin, skeletal muscle, fascia, tendons and ligaments MONDO_0018231
bone disorder MONDO_0005381
otopalatodigital syndrome spectrum disorder MONDO_0018233
filamin-related bone disorder MONDO_0019690
obsolete primary bone dysplasia with micromelia MONDO_0018232
obsolete juvenile xanthogranuloma MONDO_0006259
jejunal neuroendocrine tumor G1 MONDO_0006257
jejunal neuroendocrine tumor, well differentiated, low or intermediate grade MONDO_0015064
juvenile polyp MONDO_0006258
intimal sarcoma MONDO_0006255
spindle cell sarcoma MONDO_0002927
invasive breast carcinoma MONDO_0006256
invasive carcinoma MONDO_0040677
breast carcinoma MONDO_0004989