|
1
|
(HPO:0000093)
|
Proteinuria |
|
|
|
|
169 / 7739
|
|
2
|
(HPO:0000726)
|
Dementia |
|
|
|
|
131 / 7739
|
|
3
|
(HPO:0001289)
|
Confusion |
|
|
|
|
36 / 7739
|
|
4
|
(HPO:0001889)
|
Megaloblastic anemia |
|
|
|
|
28 / 7739
|
|
5
|
(HPO:0003401)
|
Paresthesia |
|
|
|
|
42 / 7739
|
|
6
|
(HPO:0003474)
|
Sensory impairment |
|
|
|
|
54 / 7739
|
|
7
|
(HPO:0200118)
|
Malabsorption of Vitamin B12 |
|
|
|
|
3 / 7739
|
|
8
|
(OMIM)
|
Normal intrinsic factor protein |
|
|
|
|
1 / 7739
|
|
9
|
(HPO:0009830)
|
Peripheral neuropathy |
|
|
|
|
206 / 7739
|
|
10
|
(OMIM)
|
Megaloblastic anemia, chronic, relapsing |
|
|
|
|
1 / 7739
|
|
11
|
(OMIM)
|
Pernicious anemia, not influenced by intrinsic factor |
|
|
|
|
1 / 7739
|
|
12
|
(OMIM)
|
No antibodies to intrinsic factor |
|
|
|
|
1 / 7739
|
|
13
|
(OMIM)
|
Decreased levels of serum vitamin B12 |
|
|
|
|
1 / 7739
|
|
14
|
(OMIM)
|
Normal serum folate levels |
|
|
|
|
1 / 7739
|
|
15
|
(HPO:0000007)
|
Autosomal recessive inheritance |
|
|
|
|
2538 / 7739
|
|
16
|
(HPO:0011463)
|
Childhood onset |
|
|
|
|
65 / 7739
|