Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:616721	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIn; CDG2N	—	—	—
OMIM	OMIM:616722	RETINAL DYSTROPHY AND IRIS COLOBOMA WITH OR WITHOUT CONGENITAL CATARACT; RDICC	—	—	—
OMIM	OMIM:616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA	—	—	—
OMIM	OMIM:616724	TOOTH AGENESIS, SELECTIVE, 7; STHAG7	—	—	—
OMIM	OMIM:616726	CILIARY DYSKINESIA, PRIMARY, 33; CILD33	—	—	—
OMIM	OMIM:616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES; CPRF	—	—	—
OMIM	OMIM:616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11	—	—	—
OMIM	OMIM:616732	OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA, MENTAL RETARDATION, AND SEIZURES; OPA10	—	—	—
OMIM	OMIM:616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8	—	—	—
OMIM	OMIM:616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2	—	—	—
OMIM	OMIM:616736	TREMOR, HEREDITARY ESSENTIAL, 5; ETM5	—	—	—
OMIM	OMIM:616737	TAKENOUCHI-KOSAKI SYNDROME; TKS	—	—	—
OMIM	OMIM:616738	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2; RUSAT2	—	—	—
OMIM	OMIM:616739	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 51; MRT51	—	—	—
OMIM	OMIM:616740	IMMUNODEFICIENCY 46; IMD46	—	—	—
OMIM	OMIM:616744	AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE; AISBL	—	—	—
OMIM	OMIM:616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL; HTX7	—	—	—
OMIM	OMIM:616754	BOMBAY PHENOTYPE	—	—	—
OMIM	OMIM:616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES; SPPRS	—	—	—
OMIM	OMIM:616760	WOOLLY HAIR, AUTOSOMAL RECESSIVE 3; ARWH3	—	—	—
OMIM	OMIM:616763	LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA; LDAMD	—	—	—
OMIM	OMIM:616777	SECKEL SYNDROME 9; SCKL9	—	—	—
OMIM	OMIM:616779	CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2; CADASIL2	—	—	—
OMIM	OMIM:616780	OOCYTE MATURATION DEFECT 2; OOMD2	—	—	—
OMIM	OMIM:616781	JOUBERT SYNDROME 25; JBTS25	—	—	—