Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:616840	PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET; PARK23	—	—	—
OMIM	OMIM:616843	LYMPHEDEMA, HEREDITARY, III; LMPH3	—	—	—
OMIM	OMIM:616849	BRACHYDACTYLY, TYPE A1, D; BDA1D	—	—	—
OMIM	OMIM:616851	CATARACT 45; CTRCT45	—	—	—
OMIM	OMIM:616852	MYOPATHY, SCAPULOHUMEROPERONEAL; SHPM	—	—	—
OMIM	OMIM:616854	EVEN-PLUS SYNDROME; EVPLS	—	—	—
OMIM	OMIM:616858	COWDEN SYNDROME 7; CWS7	—	—	—
OMIM	OMIM:616859	SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA; SPAHGC	—	—	—
OMIM	OMIM:616860	ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY; SIDBA3	—	—	—
OMIM	OMIM:616863	CHROMOSOME 16p13.2 DELETION SYNDROME	—	—	—
OMIM	OMIM:616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1	—	—	—
OMIM	OMIM:616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2; SMABF2	—	—	—
OMIM	OMIM:616868	DIARRHEA 8, SECRETORY SODIUM, CONGENITAL; DIAR8	—	—	—
OMIM	OMIM:616871	MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO; MPLPF	—	—	—
OMIM	OMIM:616873	IMMUNODEFICIENCY, COMMON VARIABLE, 13; CVID13	—	—	—
OMIM	OMIM:616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR	—	—	—
OMIM	OMIM:616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN	—	—	—
OMIM	OMIM:616881	LEUKODYSTROPHY, HYPOMYELINATING, 13; HLD13	—	—	—
OMIM	OMIM:616882	ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 3; FASPS3	—	—	—
OMIM	OMIM:616887	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 52; MRT52	—	—	—
OMIM	OMIM:616890	SPLIT-FOOT MALFORMATION WITH MESOAXIAL POLYDACTYLY; SFMMP	—	—	—
OMIM	OMIM:616892	NEPHROTIC SYNDROME, TYPE 12; NPHS12	—	—	—
OMIM	OMIM:616893	NEPHROTIC SYNDROME, TYPE 13; NPHS13	—	—	—
OMIM	OMIM:616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3; DRS3	—	—	—
OMIM	OMIM:616896	MITOCHONDRIAL DNA DEPLETION SYNDROME 14 (CARDIOENCEPHALOMYOPATHIC TYPE); MTDPS14	—	—	—