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All terms in MONDO

Label Id Description
hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 MONDO_0100083
hereditary thrombocytopenia and hematologic cancer predisposition syndrome MONDO_0011071
alpha-actinopathy MONDO_0100084
cancer of long bone of upper limb MONDO_0100085
cancer affecting bone of limb skeleton MONDO_0024311
perinatal disease MONDO_0100086
familial Alzheimer disease MONDO_0100087
obsolete late-onset familial alzheimer disease MONDO_0100088
GATA1-Related X-Linked Cytopenia MONDO_0100089
hematologic disorder MONDO_0005570
autoimmune thyroid disease, susceptibility to, 5 MONDO_0800261
myopathy, congenital, with excess of muscle spindles MONDO_0800299
neuronal ceroid lipofuscinosis, late infantile MONDO_0800297
peroxisome biogenesis disorder, complementation group 2 MONDO_0800298
Usher syndrome, type 1D/F MONDO_0100050
idiopathic mast cell activation syndrome MONDO_0100051
acetazolamide-responsive hereditary episodic ataxia MONDO_0100052
anaphylaxis MONDO_0100053
hypersensitivity reaction disease MONDO_0000605
idiopathic anaphylaxis MONDO_0100054