Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:616399	BRUGADA SYNDROME 9; BRGDA9	—	—	—
OMIM	OMIM:616400	PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL 2; FNEPPK2	—	—	—
OMIM	OMIM:616402	MICROCEPHALY 14, PRIMARY, AUTOSOMAL RECESSIVE; MCPH14	—	—	—
OMIM	OMIM:616407	BROWN SYNDROME; BRWNS	—	—	—
OMIM	OMIM:616409	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 33; EIEE33	—	—	—
OMIM	OMIM:616410	SPINOCEREBELLAR ATAXIA 41; SCA41	—	—	—
OMIM	OMIM:616411	DYSTONIA 27; DYT27	—	—	—
OMIM	OMIM:616413	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6; IBGC6	—	—	—
OMIM	OMIM:616414	AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE; AILJK	—	—	—
OMIM	OMIM:616415	FAMILIAL ADENOMATOUS POLYPOSIS 3; FAP3	—	—	—
OMIM	OMIM:616418	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION; HOMGSMR	—	—	—
OMIM	OMIM:616420	LEUKODYSTROPHY, HYPOMYELINATING, 10; HLD10	—	—	—
OMIM	OMIM:616421	MYOCLONIC-ATONIC EPILEPSY; MAE	—	—	—
OMIM	OMIM:616425	46,XY SEX REVERSAL 10; SRXY10	—	—	—
OMIM	OMIM:616428	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 10; MCOPCB10	—	—	—
OMIM	OMIM:616430	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25	—	—	—
OMIM	OMIM:616433	IMMUNODEFICIENCY 40; IMD40	—	—	—
OMIM	OMIM:616435	FANCONI ANEMIA, COMPLEMENTATION GROUP T; FANCT	—	—	—
OMIM	OMIM:616436	EPILEPSY, FAMILIAL TEMPORAL LOBE, 7; ETL7	—	—	—
OMIM	OMIM:616437	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3	—	—	—
OMIM	OMIM:616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4	—	—	—
OMIM	OMIM:616445	CANDIDIASIS, FAMILIAL, 9; CANDF9	—	—	—
OMIM	OMIM:616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS	—	—	—
OMIM	OMIM:616451	SPASTIC PARAPLEGIA 74, AUTOSOMAL RECESSIVE; SPG74	—	—	—
OMIM	OMIM:616452	B-CELL EXPANSION WITH NFKB AND T-CELL ANERGY; BENTA	—	—	—