Db
|
Link
|
Name
|
Definition
|
Comment
|
Is a
|
OMIM |
OMIM:102920 |
REMOVED FROM DATABASE |
— |
— |
— |
OMIM |
OMIM:102930 |
REMOVED FROM DATABASE |
— |
— |
— |
OMIM |
OMIM:102940 |
REMOVED FROM DATABASE |
— |
— |
— |
OMIM |
OMIM:102970 |
REMOVED FROM DATABASE |
— |
— |
— |
OMIM |
OMIM:102990 |
MOVED TO 145600 |
— |
— |
— |
OMIM |
OMIM:103050 |
ADENYLOSUCCINASE DEFICIENCY; ADSLD |
— |
— |
— |
OMIM |
OMIM:103100 |
ADIE PUPIL |
— |
— |
— |
OMIM |
OMIM:103200 |
ADIPOSIS DOLOROSA |
— |
— |
— |
OMIM |
OMIM:103230 |
ADRENOCORTICAL HYPOFUNCTION, CHRONIC PRIMARY CONGENITAL |
— |
— |
— |
OMIM |
OMIM:103285 |
ADULT SYNDROME |
— |
— |
— |
OMIM |
OMIM:103300 |
HYPOGLOSSIA-HYPODACTYLIA |
— |
— |
— |
OMIM |
OMIM:103321 |
MOVED TO 128239 |
— |
— |
— |
OMIM |
OMIM:103400 |
AINHUM |
— |
— |
— |
OMIM |
OMIM:103420 |
ALACRIMA, CONGENITAL, AUTOSOMAL DOMINANT |
— |
— |
— |
OMIM |
OMIM:103470 |
ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS |
— |
— |
— |
OMIM |
OMIM:103500 |
TIETZ ALBINISM-DEAFNESS SYNDROME; TADS |
— |
— |
— |
OMIM |
OMIM:103580 |
PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A |
— |
— |
— |
OMIM |
OMIM:103581 |
MOVED TO 103580 |
— |
— |
— |
OMIM |
OMIM:103780 |
ALCOHOL DEPENDENCE |
— |
— |
— |
OMIM |
OMIM:103800 |
MOVED TO 253200 AND 258870 |
— |
— |
— |
OMIM |
OMIM:103900 |
HYPERALDOSTERONISM, FAMILIAL, TYPE I; HALD1 |
— |
— |
— |
OMIM |
OMIM:103920 |
ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS, FAMILIAL |
— |
— |
— |
OMIM |
OMIM:104000 |
ALOPECIA AREATA 1; AA1 |
— |
— |
— |
OMIM |
OMIM:104100 |
PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1; PPKCA1 |
— |
— |
— |
OMIM |
OMIM:104110 |
ALOPECIA, FAMILIAL FOCAL; ALPF |
— |
— |
— |