Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA	—	—	—
OMIM	OMIM:617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT	—	—	—
OMIM	OMIM:617681	BLEPHAROCHEILODONTIC SYNDROME 2; BCDS2	—	—	—
OMIM	OMIM:617682	PILAROWSKI-BJORNSSON SYNDROME; PILBOS	—	—	—
OMIM	OMIM:617686	PITUITARY ADENOMA 3, MULTIPLE TYPES; PITA3	—	—	—
OMIM	OMIM:617690	OVARIAN DYSGENESIS 5; ODG5	—	—	—
OMIM	OMIM:617691	SPINOCEREBELLAR ATAXIA 44; SCA44	—	—	—
OMIM	OMIM:617694	AL KAISSI SYNDROME; ALKAS	—	—	—
OMIM	OMIM:617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11	—	—	—
OMIM	OMIM:617698	3-METHYLGLUTACONIC ACIDURIA, TYPE IX; MGCA9	—	—	—
OMIM	OMIM:617706	SPERMATOGENIC FAILURE 22; SPGF22	—	—	—
OMIM	OMIM:617707	SPERMATOGENIC FAILURE 23; SPGF23	—	—	—
OMIM	OMIM:617709	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ATAXIA, AND SEIZURES; NEDMAS	—	—	—
OMIM	OMIM:617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS	—	—	—
OMIM	OMIM:617711	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 1; IECEE1	—	—	—
OMIM	OMIM:617712	OOCYTE MATURATION DEFECT 3; OOMD3	—	—	—
OMIM	OMIM:617713	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33; COXPD33	—	—	—
OMIM	OMIM:617717	AUDITORY NEUROPATHY AND OPTIC ATROPHY; ANOA	—	—	—
OMIM	OMIM:617718	PLATELET ABNORMALITIES WITH EOSINOPHILIA AND IMMUNE-MEDIATED INFLAMMATORY DISEASE; PLTEID	—	—	—
OMIM	OMIM:617719	EPIPHYSEAL DYSPLASIA, MULTIPLE, 7; EDM7	—	—	—
OMIM	OMIM:617721	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IX; HMN9	—	—	—
OMIM	OMIM:617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3	—	—	—
OMIM	OMIM:617730	GALLOWAY-MOWAT SYNDROME 4; GAMOS4	—	—	—
OMIM	OMIM:617731	GALLOWAY-MOWAT SYNDROME 5; GAMOS5	—	—	—
OMIM	OMIM:617732	FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD	—	—	—