Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:617217	AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA6; AI2A6	—	—	—
OMIM	OMIM:617219	CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL	—	—	—
OMIM	OMIM:617222	SUDDEN CARDIAC FAILURE, INFANTILE; SCFI	—	—	—
OMIM	OMIM:617223	SUDDEN CARDIAC FAILURE, ALCOHOL-INDUCED; SCFAI	—	—	—
OMIM	OMIM:617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE; SPG78	—	—	—
OMIM	OMIM:617228	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31; COXPD31	—	—	—
OMIM	OMIM:617232	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Z; LGMD2Z	—	—	—
OMIM	OMIM:617234	PREIMPLANTATION EMBRYONIC LETHALITY 2; PREMBL2	—	—	—
OMIM	OMIM:617235	MYOCLONUS, INTRACTABLE, NEONATAL; NEIMY	—	—	—
OMIM	OMIM:617236	CONE-ROD DYSTROPHY AND HEARING LOSS; CRDHL	—	—	—
OMIM	OMIM:617237	IMMUNODEFICIENCY 49; IMD49	—	—	—
OMIM	OMIM:617238	MYOPIA 25, AUTOSOMAL DOMINANT; MYP25	—	—	—
OMIM	OMIM:617239	MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC; CMS21	—	—	—
OMIM	OMIM:617241	LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME; LICS	—	—	—
OMIM	OMIM:617243	FANCONI ANEMIA, COMPLEMENTATION GROUP V; FANCV	—	—	—
OMIM	OMIM:617244	FANCONI ANEMIA, COMPLEMENTATION GROUP R; FANCR	—	—	—
OMIM	OMIM:617247	FANCONI ANEMIA, COMPLEMENTATION GROUP U; FANCU	—	—	—
OMIM	OMIM:617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8	—	—	—
OMIM	OMIM:617251	UNCOMBABLE HAIR SYNDROME 2; UHS2	—	—	—
OMIM	OMIM:617252	UNCOMBABLE HAIR SYNDROME 3; UHS3	—	—	—
OMIM	OMIM:617253	SECKEL SYNDROME 10; SCKL10	—	—	—
OMIM	OMIM:617255	LISSENCEPHALY 8; LIS8	—	—	—
OMIM	OMIM:617258	MYOPATHY, MYOFIBRILLAR, 8; MFM8	—	—	—
OMIM	OMIM:617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF	—	—	—
OMIM	OMIM:617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL	—	—	—