All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02103 - hormone deficiency, thyrotropin-releasing 275120 AR - - TRH - -
05906 CHNG7 hypothyroidism, congenital, nongoitrous, type 7 (CHNG7) 618573 AR - - TRHR - -
04634 IMNEPD multisystem neurologic, endocrine, and pancreatic disease, infantile-onset (IMNEPD) 616263 AR 1 1 PTRH2 - -
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