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All terms in MONDO

Label Id Description
cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome MONDO_0011038
renal dysplasia, cystic, susceptibility to MONDO_0011037
Lynch syndrome 4 MONDO_0013699
atrophia maculosa varioliformis cutis, familial MONDO_0011039
isolated mesenteric vein thrombosis MONDO_0035009
isolated splenic vein thrombosis MONDO_0035008
Pitt-Hopkins-like syndrome 2 MONDO_0013690
inflammatory skin and bowel disease, neonatal, 1 MONDO_0013693
epithelial basolateral chloride conductance regulator, rabbit, homolog of MONDO_0011030
intellectual disability, autosomal recessive 31 MONDO_0013694
serine biosynthesis pathway deficiency, infantile/juvenile form MONDO_0035004
autosomal dominant nonsyndromic hearing loss 11 MONDO_0011032
Feingold syndrome type 2 MONDO_0013691
BAP1-related tumor predisposition syndrome MONDO_0013692
autosomal dominant nonsyndromic hearing loss 10 MONDO_0011031
isolated inherited retinal disorder MONDO_0035002
neonatal dacryocystitis MONDO_0023023
dwarfism deafness retinitis pigmentosa MONDO_0023020
dwarfism lethal type advanced bone age MONDO_0023021
dwarfism thin bones multiple fractures MONDO_0023022