Search results for adenosylcobalamin

59 hits were found for adenosylcobalamin

# Family MCID Name MIFTS Score
1
c MTH034 Methylmalonic Aciduria, Vitamin B12-Responsive, Due to Defect in Synthesis of Adenosylcobalamin, Cblb Complementation Type 28 4.261
2
P MTH008 Methylmalonic Acidemia 49 4.211
3
VTM024 Vitamin B12-Responsive Methylmalonic Acidemia 21 3.631
4
MTH056 Methylmalonic Aciduria and Homocystinuria, Cblf Type 27 3.072
5
c MNT149 Mental Retardation, X-Linked 3 29 2.936
6
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 46 2.267
7
P MTH033 Methylmalonic Aciduria, Vitamin B12-Responsive 42 2.208
8
MTH055 Methylmalonic Aciduria and Homocystinuria, Cbld Type 31 2.208
9
MTH051 Methylmalonic Aciduria and Homocystinuria, Cblj Type 22 2.208
10
MTH021 Methylmalonic Acidemia with Homocystinuria 37 2.076
11
MTH066 Methylmalonic Acidemia with Homocystinuria Type Cbld 20 2.076
12
MTH067 Methylmalonic Acidemia with Homocystinuria Type Cblj 7 2.076
13
MTH065 Methylmalonic Acidemia Cb1a Type 5 2.076
14
MTH032 Methylmalonic Aciduria Due to Transcobalamin Receptor Defect 18 0.093
15
P CHR071 Charcot-Marie-Tooth Disease 67 0.066
16
DRM006 Dermatitis 66 0.066
17
P ATP001 Atopic Dermatitis 62 0.066
18
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 58 0.066
19
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.066
20
P ATX004 Ataxia 53 0.066
21
TTH006 Tooth Disease 52 0.066
22
NRP015 Neuropathy, Congenital Hypomyelinating 52 0.066
23
c CHR537 Charcot-Marie-Tooth Disease, Type 1e 50 0.066
24
RSS002 Roussy-Levy Syndrome 50 0.066
25
P HMC002 Homocystinuria 50 0.066
26
THR013 Thoracic Outlet Syndrome 50 0.066
27
HPT074 Hepatic Adenoma, Somatic 50 0.066
28
c CHR527 Charcot-Marie-Tooth Disease, Type 1b 49 0.066
29
c CHR532 Charcot-Marie-Tooth Disease, Type 2e 49 0.066
30
P INT063 Intellectual Disability 49 0.066
31
DJR004 Dejerine-Sottas Disease 46 0.066
32
c CHR530 Charcot-Marie-Tooth Disease, Type 2b 40 0.066
33
P HYP265 Hypotonia 38 0.066
34
c CHR534 Charcot-Marie-Tooth Disease, Type 1d 38 0.066
35
NRP016 Neuropathy, Recurrent, with Pressure Palsies 38 0.066
36
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 38 0.066
37
MTR007 Motor Peripheral Neuropathy 37 0.066
38
c CHR535 Charcot-Marie-Tooth Disease, Type 1c 37 0.066
39
BRC011 Brachial Plexus Neuropathy 36 0.066
40
ALR002 Al-Raqad Syndrome 36 0.066
41
c CHR350 Charcot-Marie-Tooth Disease, Axonal, Type 2k 36 0.066
42
ADP007 Adie Pupil 34 0.066
43
c HRD094 Hereditary Motor and Sensory Neuropathy, Type Iic 34 0.066
44
c CHR353 Charcot-Marie-Tooth Disease, Axonal, Type 2l 34 0.066
45
MTH039 Methylmalonic Aciduria, Mut(0) Type 34 0.066
46
c CHR528 Charcot-Marie-Tooth Disease, Type 2j 32 0.066
47
c DST027 Distal Hereditary Motor Neuropathy, Type Ii 30 0.066
48
c CHR529 Charcot-Marie-Tooth Disease, Type 2i 30 0.066
49
AMY003 Amyotrophic Neuralgia 27 0.066
50
c CHR352 Charcot-Marie-Tooth Disease, Axonal, Type 2f 27 0.066
51
HNM002 Hinman Syndrome 25 0.066
52
P DST003 Distal Hereditary Motor Neuropathy 25 0.066
53
ISL099 Isolated Methylmalonic Acidemia 21 0.066
54
ATX038 Ataxia and Polyneuropathy, Adult-Onset 21 0.066
55
CBL006 Cblf 20 0.066
56
c CHR549 Charcot-Marie-Tooth Disease Type 2l 17 0.066
57
AND005 Androgen Insensitivity Syndrome, Mild 16 0.066
58
MNC020 Monoclonal Mast Cell Activation Syndrome 12 0.066
59
c CHR305 Charcot-Marie-Tooth Neuropathy Type 2l 11 0.066
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