|
1
|
(HPO:0001051)
|
Seborrheic dermatitis |
|
|
|
|
25 / 7739
|
|
2
|
(HPO:0001252)
|
Muscular hypotonia |
|
|
|
|
990 / 7739
|
|
3
|
(HPO:0001324)
|
Muscle weakness |
|
|
|
|
859 / 7739
|
|
4
|
(HPO:0001596)
|
Alopecia |
|
|
|
|
162 / 7739
|
|
5
|
(HPO:0001992)
|
Organic aciduria |
|
|
|
|
28 / 7739
|
|
6
|
(HPO:0001993)
|
Ketoacidosis |
|
|
|
|
17 / 7739
|
|
7
|
(HPO:0003108)
|
Hyperglycinuria |
|
|
|
|
11 / 7739
|
|
8
|
(HPO:0003202)
|
Skeletal muscle atrophy |
|
|
|
|
281 / 7739
|
|
9
|
(HPO:0003353)
|
Propionyl-CoA carboxylase deficiency |
|
|
|
|
2 / 7739
|
|
10
|
(HPO:0008947)
|
Infantile muscular hypotonia |
|
|
|
|
482 / 7739
|
|
11
|
(HPO:0010547)
|
Muscle flaccidity |
|
|
|
|
466 / 7739
|
|
12
|
(OMIM)
|
3-methylcrotonyl-CoA-carboxylase deficiency |
|
|
|
|
1 / 7739
|
|
13
|
(OMIM)
|
Beta-methylcrotonylglycinuria |
|
|
|
|
1 / 7739
|
|
14
|
(OMIM)
|
Tiglycinuria |
|
|
|
|
1 / 7739
|
|
15
|
(MedDRA:10003694)
|
Atrophy |
|
|
|
|
7 / 7739
|
|
16
|
(HPO:0000007)
|
Autosomal recessive inheritance |
|
|
|
|
2538 / 7739
|