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All terms in MONDO

Label Id Description
mast cell neoplasm MONDO_0002724
autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency MONDO_0014710
progressive microcephaly-seizures-cortical blindness-developmental delay syndrome MONDO_0014714
porokeratosis 9, multiple types MONDO_0014713
disseminated superficial actinic porokeratosis MONDO_0019212
Senior-Loken syndrome 9 MONDO_0014712
autosomal dominant Charcot-Marie-Tooth disease type 2W MONDO_0014711
rhabdoid tumor of the kidney MONDO_0002729
obsolete diffuse cutaneous mastocytosis MONDO_0002725
cutaneous solitary mastocytoma MONDO_0002726
obsolete MONDO:0002733 MONDO_0002733
anal mucinous adenocarcinoma MONDO_0002734
rectum mucinous adenocarcinoma MONDO_0002748
kidney neoplasm MONDO_0021163
14q32 duplication syndrome MONDO_0014707
partial duplication of the long arm of chromosome 14 MONDO_0016964
cutis laxa, autosomal dominant 3 MONDO_0014706
autosomal dominant cutis laxa MONDO_0019571
craniosynostosis 6 MONDO_0014705
skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome MONDO_0014704