|
Legend |

 ID
|

 Abbreviation
|

 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 |
- |
- |
|
Legend |