| OMIM |
OMIM:617862 |
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY; NEDMEBA |
— |
— |
— |
| OMIM |
OMIM:617864 |
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES; NEDSGA |
— |
— |
— |
| OMIM |
OMIM:617865 |
NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA |
— |
— |
— |
| OMIM |
OMIM:617866 |
SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY; SRTD18 |
— |
— |
— |
| OMIM |
OMIM:617871 |
RETINITIS PIGMENTOSA 81; RP81 |
— |
— |
— |
| OMIM |
OMIM:617872 |
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 34; COXPD34 |
— |
— |
— |
| OMIM |
OMIM:617873 |
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35; COXPD35 |
— |
— |
— |
| OMIM |
OMIM:617874 |
POLYCYSTIC LIVER DISEASE 3 WITH OR WITHOUT KIDNEY CYSTS; PCLD3 |
— |
— |
— |
| OMIM |
OMIM:617875 |
POLYCYSTIC LIVER DISEASE 4 WITH OR WITHOUT KIDNEY CYSTS; PCLD4 |
— |
— |
— |
| OMIM |
OMIM:617877 |
SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC |
— |
— |
— |
| OMIM |
OMIM:617879 |
LEBER CONGENITAL AMAUROSIS WITH EARLY-ONSET DEAFNESS; LCAEOD |
— |
— |
— |
| OMIM |
OMIM:617882 |
CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G; CMTDIG |
— |
— |
— |
| OMIM |
OMIM:617883 |
FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS |
— |
— |
— |
| OMIM |
OMIM:617885 |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 19; BMIQ19 |
— |
— |
— |
| OMIM |
OMIM:617892 |
AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 24; ALS24 |
— |
— |
— |
| OMIM |
OMIM:617895 |
SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19 |
— |
— |
— |
| OMIM |
OMIM:617898 |
MULTIPLE SYNOSTOSES SYNDROME 4; SYNS4 |
— |
— |
— |
| OMIM |
OMIM:617899 |
LEUKODYSTROPHY, HYPOMYELINATING, 14; HLD14 |
— |
— |
— |
| OMIM |
OMIM:617900 |
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 8; IIAE8 |
— |
— |
— |
| OMIM |
OMIM:617903 |
NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS; NDPLHS |
— |
— |
— |
| OMIM |
OMIM:617904 |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 59; EIEE59 |
— |
— |
— |
| OMIM |
OMIM:617907 |
ERYTHROCYTOSIS, FAMILIAL, 5; ECYT5 |
— |
— |
— |
| OMIM |
OMIM:617911 |
DIAMOND-BLACKFAN ANEMIA-LIKE; DBAL |
— |
— |
— |
| OMIM |
OMIM:617912 |
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5; CHTD5 |
— |
— |
— |
| OMIM |
OMIM:617913 |
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR |
— |
— |
— |