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All terms in MONDO

Label Id Description
visceral steatosis, congenital MONDO_0009220
thrombophilia, familial, due to decreased release of tissue plasminogen activator MONDO_0012872
Ehlers-Danlos syndrome, spondylocheirodysplastic type MONDO_0012873
chromosome 2q31.2 deletion syndrome MONDO_0012870
xeroderma pigmentosum group C MONDO_0010211
Jervell and Lange-Nielsen syndrome 2 MONDO_0012871
long QT syndrome 5 MONDO_0013372
xeroderma pigmentosum group A MONDO_0010210
heparin cofactor 2 deficiency MONDO_0012876
xeroderma pigmentosum group E MONDO_0010213
major affective disorder 8 MONDO_0012877
xeroderma pigmentosum group D MONDO_0010212
xeroderma pigmentosum group F MONDO_0010215
porokeratosis 6, disseminated superficial actinic type MONDO_0012874
inflammatory bowel disease 21 MONDO_0012875
xeroderma pigmentosum variant type MONDO_0010214
haemophilus meningitis MONDO_0000889
mucinous bronchioloalveolar adenocarcinoma MONDO_0000894
lung colloid adenocarcinoma MONDO_0027772
mixed mucinous and nonmucinous bronchioloalveolar adenocarcinoma MONDO_0000893