Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:616005	IMMUNODEFICIENCY 36; IMD36	—	—	—
OMIM	OMIM:616006	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2	—	—	—
OMIM	OMIM:616007	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA; CAGSSS	—	—	—
OMIM	OMIM:616018	REMOVED FROM DATABASE	—	—	—
OMIM	OMIM:616022	NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE; SCN6	—	—	—
OMIM	OMIM:616025	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 11; GPIBD11	—	—	—
OMIM	OMIM:616026	FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG; FRTS4	—	—	—
OMIM	OMIM:616028	ADAMS-OLIVER SYNDROME 5; AOS5	—	—	—
OMIM	OMIM:616029	ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME; ECTDS	—	—	—
OMIM	OMIM:616030	HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA; HH22	—	—	—
OMIM	OMIM:616032	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8; FSGS8	—	—	—
OMIM	OMIM:616033	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1; MSSGM1	—	—	—
OMIM	OMIM:616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD	—	—	—
OMIM	OMIM:616037	CILIARY DYSKINESIA, PRIMARY, 30; CILD30	—	—	—
OMIM	OMIM:616038	NEU-LAXOVA SYNDROME 2; NLS2	—	—	—
OMIM	OMIM:616039	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D; CMTRID	—	—	—
OMIM	OMIM:616040	MYASTHENIC SYNDROME, CONGENITAL, 7, PRESYNAPTIC; CMS7	—	—	—
OMIM	OMIM:616042	DEAFNESS, AUTOSOMAL RECESSIVE 103; DFNB103	—	—	—
OMIM	OMIM:616044	DEAFNESS, AUTOSOMAL DOMINANT 65; DFNA65	—	—	—
OMIM	OMIM:616045	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22; COXPD22	—	—	—
OMIM	OMIM:616050	AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS; AIFEC	—	—	—
OMIM	OMIM:616051	MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE; MCPH13	—	—	—
OMIM	OMIM:616052	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7; MDDGC7	—	—	—
OMIM	OMIM:616053	SPINOCEREBELLAR ATAXIA 40; SCA40	—	—	—
OMIM	OMIM:616055	EPISODIC ATAXIA, TYPE 8; EA8	—	—	—