| OMIM |
OMIM:124060 |
CYTOCHROME P450, SUBFAMILY I, POLYPEPTIDE 2; CYP1A2 |
— |
— |
— |
| OMIM |
OMIM:124100 |
DANUBIAN ENDEMIC FAMILIAL NEPHROPATHY |
— |
— |
— |
| OMIM |
OMIM:124200 |
DARIER-WHITE DISEASE; DAR |
— |
— |
— |
| OMIM |
OMIM:124300 |
DARWINIAN TUBERCLE OF PINNA |
— |
— |
— |
| OMIM |
OMIM:124400 |
DARWINIAN TUBERCLE OF PINNA |
— |
— |
— |
| OMIM |
OMIM:124480 |
DEAFNESS, CONGENITAL, WITH ONYCHODYSTROPHY, AUTOSOMAL DOMINANT; DDOD |
— |
— |
— |
| OMIM |
OMIM:124490 |
DEAFNESS, CONDUCTIVE STAPEDIAL, WITH EAR MALFORMATION AND FACIAL PALSY |
— |
— |
— |
| OMIM |
OMIM:124500 |
VOHWINKEL SYNDROME; VOWNKL |
— |
— |
— |
| OMIM |
OMIM:124580 |
REMOVED FROM DATABASE |
— |
— |
— |
| OMIM |
OMIM:124700 |
DEAFNESS, MID-TONE NEURAL |
— |
— |
— |
| OMIM |
OMIM:124800 |
MOVED TO 600994 |
— |
— |
— |
| OMIM |
OMIM:124900 |
DEAFNESS, AUTOSOMAL DOMINANT 1; DFNA1 |
— |
— |
— |
| OMIM |
OMIM:124910 |
MOVED TO 124900 |
— |
— |
— |
| OMIM |
OMIM:124950 |
DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE |
— |
— |
— |
| OMIM |
OMIM:125000 |
DEAFNESS, UNILATERAL |
— |
— |
— |
| OMIM |
OMIM:125050 |
DEAFNESS WITH ANHIDROTIC ECTODERMAL DYSPLASIA |
— |
— |
— |
| OMIM |
OMIM:125100 |
MOVED TO 602588 |
— |
— |
— |
| OMIM |
OMIM:125230 |
DEAFNESS-CRANIOFACIAL SYNDROME |
— |
— |
— |
| OMIM |
OMIM:125250 |
OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY |
— |
— |
— |
| OMIM |
OMIM:125260 |
DEFECTIVE INTERFERING PARTICLE INDUCTION, CONTROL OF |
— |
— |
— |
| OMIM |
OMIM:125280 |
DENS EVAGINATUS |
— |
— |
— |
| OMIM |
OMIM:125300 |
DENS IN DENTE AND PALATAL INVAGINATIONS |
— |
— |
— |
| OMIM |
OMIM:125310 |
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1; CADASIL1 |
— |
— |
— |
| OMIM |
OMIM:125320 |
DEMENTIA/PARKINSONISM WITH NON-ALZHEIMER AMYLOID PLAQUES |
— |
— |
— |
| OMIM |
OMIM:125350 |
FAILURE OF TOOTH ERUPTION, PRIMARY; PFE |
— |
— |
— |