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All terms in MONDO

Label Id Description
epiphyseal dysplasia, multiple, 3 MONDO_0010964
multiple epiphyseal dysplasia due to collagen 9 anomaly MONDO_0015627
choreoathetosis, familial inverted MONDO_0007325
retinopathy, pigmentary, and intellectual disability MONDO_0009986
autosomal recessive nonsyndromic hearing loss 7 MONDO_0010967
retinohepatoendocrinologic syndrome MONDO_0009985
chondrodysplasia punctata, tibial-metacarpal type MONDO_0007322
autosomal dominant chondrodysplasia punctata MONDO_0007321
achondrogenesis type IB MONDO_0010966
Chondronectin MONDO_0007323
late-adult onset retinitis pigmentosa MONDO_0009984
cone-rod dystrophy 5 MONDO_0010969
retinitis pigmentosa-intellectual disability-deafness-hypogenitalism syndrome MONDO_0009983
chondrocalcinosis due to apatite crystal deposition MONDO_0007320
glaucoma 3, primary infantile, B MONDO_0010968
retinitis pigmentosa inversa with deafness MONDO_0009982
obsolete retinitis pigmentosa type 1 MONDO_0009981
retinal telangiectasia and hypogammaglobulinemia MONDO_0009980
Revesz syndrome MONDO_0009990
obsolete Landau-Kleffner syndrome MONDO_0020309