Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:616649	SPHEROCYTOSIS, TYPE 2; SPH2	—	—	—
OMIM	OMIM:616651	ROIFMAN SYNDROME; RFMN	—	—	—
OMIM	OMIM:616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL	—	—	—
OMIM	OMIM:616654	JOUBERT SYNDROME 24; JBTS24	—	—	—
OMIM	OMIM:616657	SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY; SPATCCM	—	—	—
OMIM	OMIM:616668	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X; CMT2X	—	—	—
OMIM	OMIM:616669	IMMUNODEFICIENCY 45; IMD45	—	—	—
OMIM	OMIM:616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27	—	—	—
OMIM	OMIM:616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE; SPG75	—	—	—
OMIM	OMIM:616681	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE; MCPH16	—	—	—
OMIM	OMIM:616682	SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME; SSMS	—	—	—
OMIM	OMIM:616683	LEUKODYSTROPHY, HYPOMYELINATING, 12; HLD12	—	—	—
OMIM	OMIM:616684	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K; CMT4K	—	—	—
OMIM	OMIM:616685	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 14; EIG14	—	—	—
OMIM	OMIM:616687	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Y; CMT2Y	—	—	—
OMIM	OMIM:616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z	—	—	—
OMIM	OMIM:616689	DEHYDRATED HEREDITARY STOMATOCYTOSIS 2; DHS2	—	—	—
OMIM	OMIM:616697	DEAFNESS, AUTOSOMAL DOMINANT 69; DFNA69	—	—	—
OMIM	OMIM:616705	DEAFNESS, AUTOSOMAL RECESSIVE 97; DFNB97	—	—	—
OMIM	OMIM:616707	DEAFNESS, AUTOSOMAL DOMINANT 68; DFNA68	—	—	—
OMIM	OMIM:616708	DESANTO-SHINAWI SYNDROME; DESSH	—	—	—
OMIM	OMIM:616710	PARKINSON DISEASE 22, AUTOSOMAL DOMINANT; PARK22	—	—	—
OMIM	OMIM:616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5	—	—	—
OMIM	OMIM:616719	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21; SCAR21	—	—	—
OMIM	OMIM:616720	MYASTHENIC SYNDROME, CONGENITAL, 19; CMS19	—	—	—