Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:615974	DEAFNESS, AUTOSOMAL RECESSIVE 102; DFNB102	—	—	—
OMIM	OMIM:615978	IMMUNODEFICIENCY 27B; IMD27B	—	—	—
OMIM	OMIM:615979	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 45; MRT45	—	—	—
OMIM	OMIM:615980	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6; FPLD6	—	—	—
OMIM	OMIM:615981	BARDET-BIEDL SYNDROME 2; BBS2	—	—	—
OMIM	OMIM:615982	BARDET-BIEDL SYNDROME 4; BBS4	—	—	—
OMIM	OMIM:615983	BARDET-BIEDL SYNDROME 5; BBS5	—	—	—
OMIM	OMIM:615984	BARDET-BIEDL SYNDROME 7; BBS7	—	—	—
OMIM	OMIM:615985	BARDET-BIEDL SYNDROME 8; BBS8	—	—	—
OMIM	OMIM:615986	BARDET-BIEDL SYNDROME 9; BBS9	—	—	—
OMIM	OMIM:615987	BARDET-BIEDL SYNDROME 10; BBS10	—	—	—
OMIM	OMIM:615988	BARDET-BIEDL SYNDROME 11; BBS11	—	—	—
OMIM	OMIM:615989	BARDET-BIEDL SYNDROME 12; BBS12	—	—	—
OMIM	OMIM:615990	BARDET-BIEDL SYNDROME 13; BBS13	—	—	—
OMIM	OMIM:615991	BARDET-BIEDL SYNDROME 14; BBS14	—	—	—
OMIM	OMIM:615992	BARDET-BIEDL SYNDROME 15; BBS15	—	—	—
OMIM	OMIM:615993	BARDET-BIEDL SYNDROME 16; BBS16	—	—	—
OMIM	OMIM:615994	BARDET-BIEDL SYNDROME 17; BBS17	—	—	—
OMIM	OMIM:615995	BARDET-BIEDL SYNDROME 18; BBS18	—	—	—
OMIM	OMIM:615996	BARDET-BIEDL SYNDROME 19; BBS19	—	—	—
OMIM	OMIM:615999	HYPERTHYROXINEMIA, FAMILIAL DYSALBUMINEMIC; FDAH	—	—	—
OMIM	OMIM:616000	ANALBUMINEMIA; ANALBA	—	—	—
OMIM	OMIM:616001	BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 2; BNAH2	—	—	—
OMIM	OMIM:616002	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7; FSGS7	—	—	—
OMIM	OMIM:616004	DYSFIBRINOGENEMIA, CONGENITAL	—	—	—