PubDictionaries

MONDO_bioport_pref_name

183,974 entries

Label	Id

Carnitine Palmitoyltransferase 2 deficiency, infantile	10914
torsion dystonia 2, autosomal recessive type	9141
CADASIL type 1	914
Meier-GORLIN syndrome 1	9143
Meier-Gorlin syndrome 1	9143
SPERMATOGENIC FAILURE 33	29147
spermatogenic failure 33	29147
SPERMATOGENIC FAILURE 33; SPGF33	http://purl.obolibrary.org/obo/MONDO_0029147
SPERMATOGENIC FAILURE 34	29148
spermatogenic failure 34	29148
SPERMATOGENIC FAILURE 34; SPGF34	http://purl.obolibrary.org/obo/MONDO_0029148
GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18	http://purl.obolibrary.org/obo/MONDO_0029140
CARNITINE PALMITOYLTRANSFERASE II deficiency, infantile	10914
Meier-GORLIN syndrome 1; MGORS1	http://purl.obolibrary.org/obo/MONDO_0009143
torsion dystonia 2	9141