All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00106 CCHS Central hypoventilation syndrome 209880 - 0 0 PHOX2B, RET - -
00131 HSCR1 Hirschsprung disease, susceptibility to, 1 142623 - 0 0 RET - -
00129 MEN2A Multiple endocrine neoplasia IIA 171400 - 0 0 RET - -
00130 MEN2B Multiple endocrine neoplasia IIB 162300 - 0 0 RET - -
00128 MTC Medullary thyroid carcinoma, familial 155240 - 0 0 RET thyroid gland -
00087 Pheo Pheochromocytoma, susceptibility to 171300 - 23 23 MAX, RET, SDHB, SDHD, TMEM127, VHL - -
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