All terms in OMIM

Label Id Description
EIF5B 606086
PBRM1 606083
CDC42EP1 606084
BCYRN1 606089
SYNM 606087
PLA2G4B 606088
pseudomonilethrix 177750
SLC2A2 138160
intellectual developmental disorder, autosomal dominant 57 618050
cardiomyopathy, familial hypertrophic, 27 618052
Cardiomyopathy, familial hypertrophic PS192600
INAVA 618051
nevus flammeus of nape of neck 163100
MINAR1 618054
ARLNC1 618053
neurodevelopmental disorder with cerebellar atrophy and with or without seizures 618056
CREG1 618055
CFAP300 618058
drug metabolism, altered, ces1-related 618057
WDR25 618059