Search results for "cblf"

The MalaCard for "cblf" has been retired.
Searching MalaCards for entries containing "cblf"

48 hits were found for 'cblf'

# Family MCID Name MIFTS Score
1
MTH056 Methylmalonic Aciduria and Homocystinuria, Cblf Type 33 11.001
2
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 38 0.093
3
P SCH015 Schizophrenia 79 0.066
4
CDS001 Cadasil 73 0.066
5
P ANG001 Angelman Syndrome 66 0.066
6
P MTH008 Methylmalonic Acidemia 63 0.066
7
c MTB001 Metabolic Syndrome X 58 0.066
8
DMN002 Dementia 58 0.066
9
P NTR004 Neutropenia 56 0.066
10
MGL001 Megaloblastic Anemia 56 0.066
11
STT001 Status Epilepticus 56 0.066
12
P THR014 Thrombocytopenia 56 0.066
13
P SZR006 Seizure Disorder 56 0.066
14
ACN002 Acanthosis Nigricans 55 0.066
15
DFC004 Deficiency Anemia 54 0.066
16
P ESP024 Esophagitis 54 0.066
17
P HMC002 Homocystinuria 52 0.066
18
P ATX004 Ataxia 50 0.066
19
c SPN225 Spondyloarthropathy 1 48 0.066
20
SCH016 Schimke Immunoosseous Dysplasia 46 0.066
21
THR013 Thoracic Outlet Syndrome 45 0.066
22
DYS073 Dysphagia 45 0.066
23
P EPL002 Epilepsy Syndrome 44 0.066
24
MCR103 Microtia 44 0.066
25
GLS007 Glossitis 43 0.066
26
STM007 Stomatitis 43 0.066
27
P PNC001 Pancytopenia 41 0.066
28
LKP003 Leukoplakia 39 0.066
29
P TRC086 Trichohepatoenteric Syndrome 1 39 0.066
30
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.066
31
TTR016 Tetra-Amelia Syndrome 36 0.066
32
P HYP265 Hypotonia 34 0.066
33
c ART101 Aortic Valve Disease 2 32 0.066
34
P ATX010 Ataxia Neuropathy Spectrum 29 0.066
35
CYS019 Cystathioninuria 30 0.066
36
NTR005 Nutritional Deficiency Disease 28 0.066
37
MTH021 Methylmalonic Acidemia with Homocystinuria 26 0.066
38
MTH039 Methylmalonic Aciduria, Mut(0) Type 26 0.066
39
CBL004 Cbld 23 0.066
40
AMN002 Amino Acid Metabolic Disorder 22 0.066
41
OCL041 Oculomotor Apraxia Cogan Type 21 0.066
42
MTH055 Methylmalonic Aciduria and Homocystinuria, Cbld Type 21 0.066
43
P MTH033 Methylmalonic Aciduria, Vitamin B12-Responsive 17 0.066
44
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 17 0.066
45
c MTH034 Methylmalonic Aciduria, Vitamin B12-Responsive, Due to Defect in Synthesis of Adenosylcobalamin, Cblb Complementation Type 16 0.066
46
MTH051 Methylmalonic Aciduria and Homocystinuria, Cblj Type 16 0.066
47
P INT105 Intellectual Disability Multi-Gene Panels 15 0.066
48
GMM005 Gamma-Cystathionase Deficiency 10 0.066