|
1
|
(HPO:0001889)
|
Megaloblastic anemia |
|
|
|
|
28 / 7739
|
|
2
|
(HPO:0002024)
|
Malabsorption |
|
|
|
|
142 / 7739
|
|
3
|
(HPO:0002715)
|
Abnormality of the immune system |
|
|
|
|
46 / 7739
|
|
4
|
(HPO:0003401)
|
Paresthesia |
|
|
|
|
42 / 7739
|
|
5
|
(HPO:0003474)
|
Sensory impairment |
|
|
|
|
54 / 7739
|
|
6
|
(HPO:0005219)
|
Absence of intrinsic factor |
|
|
|
|
3 / 7739
|
|
7
|
(HPO:0005518)
|
Erythrocyte macrocytosis |
|
|
|
|
13 / 7739
|
|
8
|
(HPO:0200118)
|
Malabsorption of Vitamin B12 |
|
|
|
|
3 / 7739
|
|
9
|
(HPO:0200143)
|
Megaloblastic erythroid hyperplasia |
|
|
|
|
1 / 7739
|
|
10
|
(OMIM)
|
Absence of intrinsic factor by immunoassay of gastric juices |
|
|
|
|
1 / 7739
|
|
11
|
(OMIM)
|
Normal gastric mucosa |
|
|
|
|
1 / 7739
|
|
12
|
(OMIM)
|
Normal gastric acid secretion |
|
|
|
|
1 / 7739
|
|
13
|
(OMIM)
|
Normal pepsin secretion |
|
|
|
|
1 / 7739
|
|
14
|
(HPO:0009830)
|
Peripheral neuropathy |
|
|
|
|
206 / 7739
|
|
15
|
(OMIM)
|
Absence of auto-antibodies to intrinsic factor or parietal cells |
|
|
|
|
1 / 7739
|
|
16
|
(OMIM)
|
Decreased serum B12 levels |
|
|
|
|
1 / 7739
|
|
17
|
(HPO:0000007)
|
Autosomal recessive inheritance |
|
|
|
|
2538 / 7739
|
|
18
|
(HPO:0003621)
|
Juvenile onset |
|
|
|
|
105 / 7739
|