| OMIM |
OMIM:617066 |
MUSCULAR DYSTROPHY, CONGENITAL, DAVIGNON-CHAUVEAU TYPE; MDCDC |
— |
— |
— |
| OMIM |
OMIM:617068 |
PORTAL HYPERTENSION, NONCIRRHOTIC; NCPH |
— |
— |
— |
| OMIM |
OMIM:617069 |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3; PEOB3 |
— |
— |
— |
| OMIM |
OMIM:617070 |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4; PEOB4 |
— |
— |
— |
| OMIM |
OMIM:617072 |
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Y; LGMD2Y |
— |
— |
— |
| OMIM |
OMIM:617073 |
TOOTH AGENESIS, SELECTIVE, 8; STHAG8 |
— |
— |
— |
| OMIM |
OMIM:617075 |
NASOPHARYNGEAL CARCINOMA, SUSCEPTIBILITY TO, 3; NPCA3 |
— |
— |
— |
| OMIM |
OMIM:617080 |
SEIZURES, BENIGN FAMILIAL INFANTILE, 5; BFIS5 |
— |
— |
— |
| OMIM |
OMIM:617082 |
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iaa; CDG1AA |
— |
— |
— |
| OMIM |
OMIM:617086 |
ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2; EMPF2 |
— |
— |
— |
| OMIM |
OMIM:617087 |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B; CMT2A2B |
— |
— |
— |
| OMIM |
OMIM:617088 |
SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15 |
— |
— |
— |
| OMIM |
OMIM:617090 |
MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE; MCPH17 |
— |
— |
— |
| OMIM |
OMIM:617091 |
CILIARY DYSKINESIA, PRIMARY, 34; CILD34 |
— |
— |
— |
| OMIM |
OMIM:617092 |
CILIARY DYSKINESIA, PRIMARY, 35; CILD35 |
— |
— |
— |
| OMIM |
OMIM:617093 |
GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY; GRIDHH |
— |
— |
— |
| OMIM |
OMIM:617099 |
AUTOINFLAMMATION, PANNICULITIS, AND DERMATOSIS SYNDROME; AIPDS |
— |
— |
— |
| OMIM |
OMIM:617100 |
FAMILIAL ADENOMATOUS POLYPOSIS 4; FAP4 |
— |
— |
— |
| OMIM |
OMIM:617101 |
INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN |
— |
— |
— |
| OMIM |
OMIM:617102 |
SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16 |
— |
— |
— |
| OMIM |
OMIM:617105 |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41 |
— |
— |
— |
| OMIM |
OMIM:617106 |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42; EIEE42 |
— |
— |
— |
| OMIM |
OMIM:617107 |
THAUVIN-ROBINET-FAIVRE SYNDROME; TROFAS |
— |
— |
— |
| OMIM |
OMIM:617108 |
SESSILE SERRATED POLYPOSIS CANCER SYNDROME; SSPCS |
— |
— |
— |
| OMIM |
OMIM:617111 |
MACULAR DYSTROPHY, PATTERNED, 3; MDPT3 |
— |
— |
— |