JSON

All terms in MONDO

Label Id Description
absent tibia-polydactyly-arachnoid cyst syndrome MONDO_0010981
benign childhood occipital epilepsy, Gastaut type MONDO_0020308
midline malformations, multiple, with limb abnormalities and hypopituitarism MONDO_0010980
benign childhood occipital epilepsy, Panayiotopoulos type MONDO_0020307
follicular atrophoderma-basal cell carcinoma MONDO_0019317
dystonia 9 MONDO_0010983
obsolete absent tibia-polydactyly syndrome MONDO_0020306
ichthyosis-intellectual disability syndrome with large keratohyalin granules in the skin MONDO_0010982
isochromosomy Yq MONDO_0020305
isochromosome Y MONDO_0019935
epilepsy, familial adult myoclonic, 1 MONDO_0010985
verrucous nevus MONDO_0019319
isochromosomy Yp MONDO_0020304
inflammatory linear verrucous epidermal nevus MONDO_0019318
Usher syndrome type 1D MONDO_0010984
Angelman syndrome due to paternal uniparental disomy of chromosome 15 MONDO_0020303
syndromic vitreoretinopathy MONDO_0034954
desmoplastic infantile ganglioglioma MONDO_0022965
obsolete syndromic inherited retinal disorder MONDO_0034953
cutaneous mastocytoma MONDO_0019314