Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:617994	TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 3; HFTC3	—	—	—
OMIM	OMIM:617995	IMPDH2 ENZYME ACTIVITY, VARIATION IN; IMPDH2V	—	—	—
OMIM	OMIM:618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2	—	—	—
OMIM	OMIM:618003	DEAFNESS, AUTOSOMAL RECESSIVE 57; DFNB57	—	—	—
OMIM	OMIM:618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64	—	—	—
OMIM	OMIM:618005	CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION; CDGF	—	—	—
OMIM	OMIM:618006	LEUKODYSTROPHY, HYPOMYELINATING, 17; HLD17	—	—	—
OMIM	OMIM:618007	NEURODEVELOPMENTAL DISORDER WITH BRAIN, LIVER, AND LUNG ABNORMALITIES; NEDBLLA	—	—	—
OMIM	OMIM:618008	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 65; EIEE65	—	—	—
OMIM	OMIM:618010	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17; GPIBD17	—	—	—
OMIM	OMIM:618011	HYPEREKPLEXIA 4; HKPX4	—	—	—
OMIM	OMIM:618012	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3; IECEE3	—	—	—
OMIM	OMIM:618013	DEAFNESS, AUTOSOMAL RECESSIVE 109; DFNB109	—	—	—
OMIM	OMIM:618014	PREMATURE OVARIAN FAILURE 14; POF14	—	—	—
OMIM	OMIM:618015	PROTOPORPHYRIA, ERYTHROPOIETIC, 2; EPP2	—	—	—
OMIM	OMIM:618018	DRUG METABOLISM, ALTERED, CYP2C8-RELATED	—	—	—
OMIM	OMIM:618019	PELGER-HUET ANOMALY WITH MILD SKELETAL ANOMALIES; PHASK	—	—	—
OMIM	OMIM:618021	TETRAAMELIA SYNDROME 2; TETAMS2	—	—	—
OMIM	OMIM:618022	HUMEROFEMORAL HYPOPLASIA WITH RADIOTIBIAL RAY DEFICIENCY; HHRRD	—	—	—
OMIM	OMIM:618026	NOTCH2 N-TERMINAL-LIKE-RELATED, PSEUDOGENE; NOTCH2NLR	—	—	—
OMIM	OMIM:618027	COFFIN-SIRIS SYNDROME 7; CSS7	—	—	—
OMIM	OMIM:618031	CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 4; PPCD4	—	—	—
OMIM	OMIM:618036	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2DD; CMT2DD	—	—	—
OMIM	OMIM:618042	PULMONARY ALVEOLAR PROTEINOSIS WITH HYPOGAMMAGLOBULINEMIA; PAPHG	—	—	—
OMIM	OMIM:618048	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 2; PRAAS2	—	—	—