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Legend |
![](gfx/trans.png)
![](gfx/order_arrow.png) ID
|
![](gfx/trans.png)
![Ascending Ascending](gfx/order_arrow_asc.png) Abbreviation
|
![](gfx/trans.png)
![](gfx/order_arrow.png) Name
|
![](gfx/trans.png)
![](gfx/order_arrow.png) OMIM ID
|
![](gfx/trans.png)
![](gfx/order_arrow.png) Inheritance
|
![](gfx/trans.png)
![](gfx/order_arrow.png) Individuals
|
![](gfx/trans.png)
![](gfx/order_arrow.png) Phenotypes
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![](gfx/trans.png) Associated with genes
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![](gfx/trans.png) Associated tissues
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![](gfx/trans.png) 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 |