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All terms in MONDO

Label Id Description
Tietz syndrome MONDO_0007077
obsolete total autosomal monosomy MONDO_0020053
alopecia-epilepsy-pyorrhea-intellectual disability syndrome MONDO_0007085
autosomal dominant Alport syndrome MONDO_0007086
autosomal dominant palmoplantar keratoderma and congenital alopecia MONDO_0007083
familial focal alopecia MONDO_0007084
obsolete allergic bronchopulmonary aspergillosis MONDO_0007081
alopecia areata 1 MONDO_0007082
neurodevelopmental disorder with absent speech and movement and behavioral abnormalities MONDO_0859519
glucocorticoid-remediable aldosteronism MONDO_0007080
neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum MONDO_0859516
obsolete syndrome with brachydactyly MONDO_0019066
obsolete rhabdoid tumor MONDO_0019069
congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization MONDO_0019068
obsolete 46,XY disorder of sex development due to a defect in testosterone metabolism by peripheral tissue MONDO_0020041
obsolete rare infectious disease MONDO_0019062
paraplegia MONDO_0003757
obsolete rare parathyroid disease and phosphocalcic metabolism anomaly MONDO_0019061
internal carotid agenesis MONDO_0020048
obsolete autosomal recessive cerebellar ataxia due to a DNA repair defect MONDO_0020045