Search results for "cblf"

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

63 hits were found for 'cblf'

# Family MCID Name MIFTS Score
1
MTH056 Methylmalonic Aciduria and Homocystinuria, Cblf Type 35 9.644
2
CBL006 Cblf 18 3.109
3
ANR002 Aniridia 72 0.088
4
ACN002 Acanthosis Nigricans 53 0.088
5
P MTH008 Methylmalonic Acidemia 52 0.088
6
THR013 Thoracic Outlet Syndrome 47 0.088
7
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 44 0.088
8
P TRC086 Trichohepatoenteric Syndrome 1 42 0.088
9
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.088
10
P ATX010 Ataxia Neuropathy Spectrum 31 0.088
11
P SCH015 Schizophrenia 79 0.062
12
CDS001 Cadasil 70 0.062
13
c SPN225 Spondyloarthropathy 1 66 0.062
14
P ANG001 Angelman Syndrome 66 0.062
15
P HRM001 Hermansky-Pudlak Syndrome 62 0.062
16
c PNC108 Pancreatitis, Hereditary 59 0.062
17
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.062
18
P EPL002 Epilepsy Syndrome 54 0.062
19
DMN002 Dementia 53 0.062
20
DFC004 Deficiency Anemia 52 0.062
21
HNT002 Hantavirus Pulmonary Syndrome 52 0.062
22
c MTB001 Metabolic Syndrome X 52 0.062
23
STT001 Status Epilepticus 51 0.062
24
SCH016 Schimke Immunoosseous Dysplasia 51 0.062
25
P CHL002 Childhood Absence Epilepsy 51 0.062
26
P ESP024 Esophagitis 51 0.062
27
P NTR004 Neutropenia 50 0.062
28
P THR014 Thrombocytopenia 50 0.062
29
GLC003 Glucose Intolerance 49 0.062
30
P SZR006 Seizure Disorder 48 0.062
31
MGL001 Megaloblastic Anemia 47 0.062
32
P HMC002 Homocystinuria 46 0.062
33
URB001 Urbach-Wiethe Disease 46 0.062
34
c ART101 Aortic Valve Disease 2 46 0.062
35
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 43 0.062
36
P ATX004 Ataxia 43 0.062
37
NTR005 Nutritional Deficiency Disease 41 0.062
38
P PNC001 Pancytopenia 41 0.062
39
MCR103 Microtia 40 0.062
40
STM007 Stomatitis 40 0.062
41
TTR016 Tetra-Amelia Syndrome 38 0.062
42
P INT063 Intellectual Disability 36 0.062
43
CRN246 Cranioosteoarthropathy 36 0.062
44
GLS007 Glossitis 36 0.062
45
P HYP265 Hypotonia 35 0.062
46
AMN002 Amino Acid Metabolic Disorder 35 0.062
47
CYS019 Cystathioninuria 34 0.062
48
DYS073 Dysphagia 33 0.062
49
LKP003 Leukoplakia 32 0.062
50
MTH039 Methylmalonic Aciduria, Mut(0) Type 31 0.062
51
UND005 Undifferentiated Pleomorphic Sarcoma 31 0.062
52
VSL002 Visual Epilepsy 31 0.062
53
MTH055 Methylmalonic Aciduria and Homocystinuria, Cbld Type 27 0.062
54
MTH021 Methylmalonic Acidemia with Homocystinuria 26 0.062
55
P MTH033 Methylmalonic Aciduria, Vitamin B12-Responsive 24 0.062
56
HMC036 Homocystinuria Without Methylmalonic Aciduria 23 0.062
57
c MTH034 Methylmalonic Aciduria, Vitamin B12-Responsive, Due to Defect in Synthesis of Adenosylcobalamin, Cblb Complementation Type 23 0.062
58
MTH051 Methylmalonic Aciduria and Homocystinuria, Cblj Type 21 0.062
59
MTH027 Mthfr Deficiency 21 0.062
60
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 19 0.062
61
OCL041 Oculomotor Apraxia Cogan Type 17 0.062
62
DSR002 Disorders of Intracellular Cobalamin Metabolism 16 0.062
63
GMM005 Gamma-Cystathionase Deficiency 10 0.062