MCID: CHR519
MIFTS: 42

Charcot-Marie-Tooth Disease, Type 4b2

Categories: Genetic diseases, Rare diseases, Neuronal diseases, Muscle diseases, Metabolic diseases, Fetal diseases, Ear diseases

Aliases & Classifications for Charcot-Marie-Tooth Disease, Type 4b2

MalaCards integrated aliases for Charcot-Marie-Tooth Disease, Type 4b2:

Name: Charcot-Marie-Tooth Disease, Type 4b2 54 29 13 69
Charcot-Marie-Tooth Disease Type 4b2 12 50 56 14
Cmt4b2 12 24 56 71
Charcot-Marie-Tooth Neuropathy Type 4b2 12 24 71
Cmt 4b2 50 24
Charcot-Marie-Tooth Disease, with Focally Folded Myelin Sheaths, Autosomal Recessive, Type 4b2 50
Autosomal Recessive Charcot-Marie-Tooth Disease with Focally Folded Myelin Sheaths Type 4b2 12
Charcot-Marie-Tooth Disease Autosomal Recessive with Focally Folded Myelin Sheaths 4b2 71
Charcot-Marie-Tooth Disease Demyelinating Autosomal Recessive 4b2 71
Charcot-Marie-Tooth Neuropathy, Type 4b2 50
Charcot Marie Tooth Disease Type 4b2 50
Charcot-Marie-Tooth Disease 4b2 71

Characteristics:

Orphanet epidemiological data:

56
charcot-marie-tooth disease type 4b2
Inheritance: Autosomal recessive; Age of onset: Childhood;

OMIM:

54
Inheritance:
autosomal recessive

Miscellaneous:
upper limb involvement usually occurs later
onset in feet and legs (peroneal distribution)
onset in first or second decade (range 4 to 13 years)
patients with glaucoma have nonsense or truncating sbf2 mutations
genetic heterogeneity (see cmt4b1, )


HPO:

32
charcot-marie-tooth disease, type 4b2:
Inheritance heterogeneous autosomal recessive inheritance
Onset and clinical course juvenile onset


Classifications:

Orphanet: 56  
Rare neurological diseases


External Ids:

OMIM 54 604563
Disease Ontology 12 DOID:0110190
ICD10 33 G60.0
Orphanet 56 ORPHA99956
MESH via Orphanet 43 C535421
UMLS via Orphanet 70 C1858278
ICD10 via Orphanet 34 G60.0
MeSH 42 D002607

Summaries for Charcot-Marie-Tooth Disease, Type 4b2

UniProtKB/Swiss-Prot : 71 Charcot-Marie-Tooth disease 4B2: A recessive demyelinating form of Charcot-Marie-Tooth disease, a disorder of the peripheral nervous system, characterized by progressive weakness and atrophy, initially of the peroneal muscles and later of the distal muscles of the arms. Charcot-Marie-Tooth disease is classified in two main groups on the basis of electrophysiologic properties and histopathology: primary peripheral demyelinating neuropathies (designated CMT1 when they are dominantly inherited) and primary peripheral axonal neuropathies (CMT2). Demyelinating neuropathies are characterized by severely reduced nerve conduction velocities (less than 38 m/sec), segmental demyelination and remyelination with onion bulb formations on nerve biopsy, slowly progressive distal muscle atrophy and weakness, absent deep tendon reflexes, and hollow feet. By convention autosomal recessive forms of demyelinating Charcot-Marie-Tooth disease are designated CMT4.

MalaCards based summary : Charcot-Marie-Tooth Disease, Type 4b2, also known as charcot-marie-tooth disease type 4b2, is related to neuropathy, congenital hypomyelinating and charcot-marie-tooth disease, and has symptoms including distal sensory impairment, hyporeflexia and kyphoscoliosis. An important gene associated with Charcot-Marie-Tooth Disease, Type 4b2 is SBF2 (SET Binding Factor 2), and among its related pathways/superpathways is RAB GEFs exchange GTP for GDP on RABs. Affiliated tissues include brain, spinal cord and eye, and related phenotype is behavior/neurological.

NIH Rare Diseases : 50 charcot-marie-tooth disease type 4b2 (cmt4b2) is a disorder that affects the peripheral nerves. peripheral nerves connect the brain and spinal cord to muscles and to sensory cells that detect sensations such as touch, pain, heat, and sound. damage to the peripheral nerves can result in loss of sensation and wasting (atrophy) of muscles in the feet, legs, and hands. cmt4b2 can also cause glaucoma (damage to the eye’s optic nerve). there is currently no cure for cmt4b2, but physical therapy, occupational therapy, braces and other orthopedic devices, pain medication, and orthopedic surgery can help manage and improve symptoms. cmt4b2 is inherited in an autosomal recessive fashion. it is caused by mutations in the sbf1 gene. last updated: 3/30/2017

OMIM : 54
Autosomal recessive Charcot-Marie-Tooth disease type 4B is a demyelinating hereditary motor and sensory neuropathy characterized by abnormal folding of myelin sheaths. CMT4B1 (601382) is a clinically similar disorder caused by mutation in the MTMR2 gene (603557) on 11q22. For a phenotypic description and a discussion of genetic heterogeneity of autosomal recessive demyelinating CMT, see CMT4A (214400). (604563)

Disease Ontology : 12 A Charcot-Marie-Tooth disease type 4 that has material basis in mutation in the SBF2 gene.

Related Diseases for Charcot-Marie-Tooth Disease, Type 4b2

Diseases in the Charcot-Marie-Tooth Disease family:

Charcot-Marie-Tooth Disease, Type 2a1 Charcot-Marie-Tooth Disease, Recessive Intermediate C
Charcot-Marie-Tooth Disease, Dominant Intermediate C Charcot-Marie-Tooth Disease, Type 2b1
Charcot-Marie-Tooth Disease, Type 1b Charcot-Marie-Tooth Disease, Type 2j
Charcot-Marie-Tooth Disease, Type 2i Charcot-Marie-Tooth Disease, Type 2b
Charcot-Marie-Tooth Disease, Type 2r Charcot-Marie-Tooth Disease, Type 4c
Charcot-Marie-Tooth Disease, Type 4j Charcot-Marie-Tooth Disease, Type 2d
Charcot-Marie-Tooth Disease, Type 2e Charcot-Marie-Tooth Disease, Type 1f
Charcot-Marie-Tooth Disease, Type 4a Charcot-Marie-Tooth Disease, Recessive Intermediate, a
Charcot-Marie-Tooth Disease, Type 4d Charcot-Marie-Tooth Disease, Type 4k
Charcot-Marie-Tooth Disease, Type 1d Charcot-Marie-Tooth Disease, Dominant Intermediate a
Charcot-Marie-Tooth Disease, Type 4b2 Charcot-Marie-Tooth Disease, Type 4b1
Charcot-Marie-Tooth Disease, Type 4h Charcot-Marie-Tooth Disease, Type 1c
Charcot-Marie-Tooth Disease, Recessive Intermediate, B Charcot-Marie-Tooth Disease, Type 1a
Charcot-Marie-Tooth Disease, Type 1e Charcot-Marie-Tooth Disease, Dominant Intermediate B
Charcot-Marie-Tooth Disease, Type 4f Charcot-Marie-Tooth Disease, Type 2b2
Charcot-Marie-Tooth Disease, Type 4b3 Charcot-Marie-Tooth Disease Intermediate Type
Charcot-Marie-Tooth Disease Type 5 Charcot-Marie-Tooth Disease Type 7
Charcot-Marie-Tooth Disease Type 2a2 Autosomal Dominant Intermediate Charcot-Marie-Tooth
Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease Type B Autosomal Recessive Intermediate Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease Type 2a Charcot-Marie-Tooth Disease Type 2c
Charcot-Marie-Tooth Disease Type 2f Charcot-Marie-Tooth Disease Type 2g
Charcot-Marie-Tooth Disease Type 2k Charcot-Marie-Tooth Disease Type 2l
Charcot-Marie-Tooth Disease Type 2n Charcot-Marie-Tooth Disease Type 2o
Charcot-Marie-Tooth Disease Type 2q Charcot-Marie-Tooth Disease Type 2b5
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due to Kif5a Mutation Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due to Tfg Mutation
Charcot-Marie-Tooth Disease Type 2t Pmp2-Related Charcot-Marie-Tooth Disease Type 1
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2w Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due to Dgat2 Mutation

Diseases related to Charcot-Marie-Tooth Disease, Type 4b2 via text searches within MalaCards or GeneCards Suite gene sharing:

(show all 21)
id Related Disease Score Top Affiliating Genes
1 neuropathy, congenital hypomyelinating 28.1 GDAP1 MTM1 MTMR2 PRX SBF1 SBF2
2 charcot-marie-tooth disease 10.4
3 tooth disease 10.4
4 hypoxia 9.7 MTMR2 PRX
5 charcot-marie-tooth neuropathy x 9.6 GDAP1 SBF2
6 congestive heart failure 9.6 MTMR2 PRX SBF2
7 pancreatic acinar cell adenocarcinoma 9.5 GDAP1 MTMR2
8 amyotrophic lateral sclerosis 11 9.2 GDAP1 MTMR2 SBF2
9 neuropathy, inflammatory demyelinating 9.2 GDAP1 MTMR2
10 familial male-limited precocious puberty 9.1 MTM1 MTMR2 SBF1 SBF2
11 dejerine-sottas disease 9.1 GDAP1 MTMR2 PRX
12 hereditary angioedema 9.1 MTM1 MTMR2 SBF1 SBF2
13 senile angioma 9.0 GDAP1 MTMR2 PRX
14 chromosome 19q13.11 deletion syndrome, distal 8.9 GDAP1 MTMR2 PRX SBF2
15 charcot-marie-tooth disease, type 1f 8.8 GDAP1 MTM1 MTMR2 SBF2
16 charcot-marie-tooth disease, axonal, with vocal cord paresis 8.8 GDAP1 MTMR2 PRX SBF2
17 short stature, idiopathic familial 8.3 GDAP1 MTM1 MTMR2 SBF1 SBF2
18 amnestic disorder 8.2 GDAP1 MTMR2 PRX SBF1 SBF2
19 hermansky-pudlak syndrome 5 7.8 GDAP1 MTM1 MTMR2 PRX SBF1 SBF2
20 progesterone resistance 7.8 GDAP1 MTM1 MTMR2 PRX SBF1 SBF2
21 childhood-onset cerebral x-linked adrenoleukodystrophy 7.7 GDAP1 MTM1 MTMR2 PRX SBF1 SBF2

Graphical network of the top 20 diseases related to Charcot-Marie-Tooth Disease, Type 4b2:



Diseases related to Charcot-Marie-Tooth Disease, Type 4b2

Symptoms & Phenotypes for Charcot-Marie-Tooth Disease, Type 4b2

Symptoms via clinical synopsis from OMIM:

54

Neurologic- Peripheral Nervous System:
distal limb muscle weakness due to peripheral neuropathy
distal limb muscle atrophy due to peripheral neuropathy
hyporeflexia
areflexia
'steppage' gait
more
Skeletal- Spine:
kyphoscoliosis may be present

Head And Neck- Ears:
sensorineural hearing loss (described in 1 family)

Skeletal- Feet:
foot deformities
pes cavus
hammertoes
talipes equinus

Skeletal- Hands:
claw hand deformities (in severe cases)

Head And Neck- Eyes:
glaucoma, open-angle, early-onset (occurs in patients with nonsense or truncating mutations in the sbf2 gene)
glaucoma may precede development of neuropathy


Clinical features from OMIM:

604563

Human phenotypes related to Charcot-Marie-Tooth Disease, Type 4b2:

32 (show all 20)
id Description HPO Frequency HPO Source Accession
1 distal sensory impairment 32 HP:0002936
2 hyporeflexia 32 HP:0001265
3 kyphoscoliosis 32 HP:0002751
4 glaucoma 32 HP:0000501
5 talipes equinovarus 32 HP:0001762
6 pes cavus 32 HP:0001761
7 areflexia 32 HP:0001284
8 steppage gait 32 HP:0003376
9 distal muscle weakness 32 HP:0002460
10 difficulty walking 32 HP:0002355
11 sensorineural hearing impairment 32 HP:0000407
12 distal amyotrophy 32 HP:0003693
13 onion bulb formation 32 HP:0003383
14 split hand 32 HP:0001171
15 decreased motor nerve conduction velocity 32 HP:0003431
16 hammertoe 32 HP:0001765
17 decreased number of peripheral myelinated nerve fibers 32 HP:0003380
18 foot dorsiflexor weakness 32 HP:0009027
19 ulnar claw 32 HP:0001178
20 segmental peripheral demyelination/remyelination 32 HP:0003481

MGI Mouse Phenotypes related to Charcot-Marie-Tooth Disease, Type 4b2:

44
id Description MGI Source Accession Score Top Affiliating Genes
1 behavior/neurological MP:0005386 9.02 GDAP1 MTM1 MTMR2 PRX SBF2

Drugs & Therapeutics for Charcot-Marie-Tooth Disease, Type 4b2

Search Clinical Trials , NIH Clinical Center for Charcot-Marie-Tooth Disease, Type 4b2

Genetic Tests for Charcot-Marie-Tooth Disease, Type 4b2

Genetic tests related to Charcot-Marie-Tooth Disease, Type 4b2:

id Genetic test Affiliating Genes
1 Charcot-Marie-Tooth Disease, Type 4b2 29
2 Charcot-Marie-Tooth Neuropathy Type 4b2 24 SBF2

Anatomical Context for Charcot-Marie-Tooth Disease, Type 4b2

MalaCards organs/tissues related to Charcot-Marie-Tooth Disease, Type 4b2:

39
Brain, Spinal Cord, Eye

Publications for Charcot-Marie-Tooth Disease, Type 4b2

Articles related to Charcot-Marie-Tooth Disease, Type 4b2:

id Title Authors Year
1
Identification of a novel SBF2 frameshift mutation in charcot-marie-tooth disease type 4B2 using whole-exome sequencing. ( 25462154 )
2014
2
Cloning, expression and characterization of the murine orthologue of SBF2, the gene mutated in Charcot-Marie-Tooth disease type 4B2. ( 16750429 )
2006

Variations for Charcot-Marie-Tooth Disease, Type 4b2

ClinVar genetic disease variations for Charcot-Marie-Tooth Disease, Type 4b2:

6
id Gene Variation Type Significance SNP ID Assembly Location
1 SBF2 SBF2, EX11-12DEL deletion Pathogenic
2 SBF2 SBF2, IVS32DS, G-C, +1 single nucleotide variant Pathogenic
3 SBF2 NM_030962.3(SBF2): c.5451+2T> G single nucleotide variant Likely pathogenic rs886042830 GRCh37 Chromosome 11, 9803052: 9803052

Expression for Charcot-Marie-Tooth Disease, Type 4b2

Search GEO for disease gene expression data for Charcot-Marie-Tooth Disease, Type 4b2.

Pathways for Charcot-Marie-Tooth Disease, Type 4b2

Pathways related to Charcot-Marie-Tooth Disease, Type 4b2 according to GeneCards Suite gene sharing:

id Super pathways Score Top Affiliating Genes
1 10.58 SBF1 SBF2

GO Terms for Charcot-Marie-Tooth Disease, Type 4b2

Cellular components related to Charcot-Marie-Tooth Disease, Type 4b2 according to GeneCards Suite gene sharing:

id Name GO ID Score Top Affiliating Genes
1 vacuolar membrane GO:0005774 8.62 MTMR2 SBF2

Biological processes related to Charcot-Marie-Tooth Disease, Type 4b2 according to GeneCards Suite gene sharing:

id Name GO ID Score Top Affiliating Genes
1 peptidyl-tyrosine dephosphorylation GO:0035335 9.37 MTM1 MTMR2
2 regulation of GTPase activity GO:0043087 9.32 SBF1 SBF2
3 protein tetramerization GO:0051262 9.26 MTMR2 SBF2
4 phosphatidylinositol dephosphorylation GO:0046856 9.16 MTM1 MTMR2
5 protein dephosphorylation GO:0006470 9.13 MTM1 MTMR2 SBF1
6 phosphatidylinositol biosynthetic process GO:0006661 8.8 MTM1 MTMR2 SBF1

Molecular functions related to Charcot-Marie-Tooth Disease, Type 4b2 according to GeneCards Suite gene sharing:

id Name GO ID Score Top Affiliating Genes
1 phosphatase activity GO:0016791 9.43 MTM1 MTMR2
2 protein tyrosine phosphatase activity GO:0004725 9.4 MTM1 MTMR2
3 phosphatidylinositol binding GO:0035091 9.37 MTM1 SBF2
4 Rab guanyl-nucleotide exchange factor activity GO:0017112 9.32 SBF1 SBF2
5 protein tyrosine/serine/threonine phosphatase activity GO:0008138 9.26 MTMR2 SBF1
6 phosphatidylinositol-3-phosphatase activity GO:0004438 9.16 MTM1 MTMR2
7 phosphatidylinositol-3,5-bisphosphate 3-phosphatase activity GO:0052629 8.96 MTM1 MTMR2
8 phosphatase regulator activity GO:0019208 8.62 SBF1 SBF2

Sources for Charcot-Marie-Tooth Disease, Type 4b2

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
16 ExPASy
18 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 MedGen
42 MeSH
43 MESH via Orphanet
44 MGI
46 NCI
47 NCIt
48 NDF-RT
51 NINDS
52 Novoseek
54 OMIM
55 OMIM via Orphanet
59 PubMed
60 QIAGEN
65 SNOMED-CT via HPO
66 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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