Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:615821	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; DCWHKTA	—	—	—
OMIM	OMIM:615824	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7; MC3DN7	—	—	—
OMIM	OMIM:615828	MENTAL RETARDATION, AUTOSOMAL DOMINANT 24; MRD24	—	—	—
OMIM	OMIM:615829	XIA-GIBBS SYNDROME	—	—	—
OMIM	OMIM:615830	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4; PPNAD4	—	—	—
OMIM	OMIM:615833	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21; EIEE21	—	—	—
OMIM	OMIM:615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26; MRD26	—	—	—
OMIM	OMIM:615835	CHROMOSOME 16 INVERSION, 0.45-MB	—	—	—
OMIM	OMIM:615837	DEAFNESS, AUTOSOMAL RECESSIVE 101; DFNB101	—	—	—
OMIM	OMIM:615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8	—	—	—
OMIM	OMIM:615841	SPERMATOGENIC FAILURE 13; SPGF13	—	—	—
OMIM	OMIM:615842	SPERMATOGENIC FAILURE 14; SPGF14	—	—	—
OMIM	OMIM:615846	AICARDI-GOUTIERES SYNDROME 7; AGS7	—	—	—
OMIM	OMIM:615848	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 10; CMM10	—	—	—
OMIM	OMIM:615849	CULLER-JONES SYNDROME; CJS	—	—	—
OMIM	OMIM:615851	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E; PCH2E	—	—	—
OMIM	OMIM:615859	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23	—	—	—
OMIM	OMIM:615860	CONE-ROD DYSTROPHY 19; CORD19	—	—	—
OMIM	OMIM:615861	NEPHROTIC SYNDROME, TYPE 10; NPHS10	—	—	—
OMIM	OMIM:615862	NEPHRONOPHTHISIS 18; NPHP18	—	—	—
OMIM	OMIM:615863	DIARRHEA 7; DIAR7	—	—	—
OMIM	OMIM:615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27; MRD27	—	—	—
OMIM	OMIM:615871	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 24; EIEE24	—	—	—
OMIM	OMIM:615872	CILIARY DYSKINESIA, PRIMARY, 29; CILD29	—	—	—
OMIM	OMIM:615873	HELSMOORTEL-VAN DER AA SYNDROME; HVDAS	—	—	—