WikiMD's Wellness Encyclopedia
WikiMD's Wellness Encyclopedia
Search
Log in
↓
Personal tools
Not logged in
Talk
Contributions
Create account
Log in
Navigation menu
Navigation
Main page
Current events
Recent changes
Popular pages
Random page
Upload file
Special pages
WikiMD St@tistics
Wellness matters
Wellness
Diet
Recipes
Weight loss diet
Medical weight loss NYC
Brooklyn weight loss
Encyclopedia
Health encyclopedia
Disease index
Health topics
Glossaries
Rare diseases
Directory
Doctor finder (US)
World Directory
Sister projects
Christian Encyclopedia
Medical weight loss NYC
Medical directory
Sponsors
NYC physician weight loss
Philadelphia medical weight loss
NYC sleep clinic
Philadelphia sleep clinic
Lose weight NYC
Indian vegetable farm NJ
W8MD weight loss centers
NYC medical weight loss
Contact
Contact us
Navigation
Speci@l PageS
Template
:
Cytoskeletal defects
From WikiMD's Wellness Encyclopedia
Revision as of 13:44, 22 January 2022 by
en>Omnipaedista
(WP:BRINT)
(diff) ← Older revision |
Latest revision
(
diff
) |
Newer revision →
(
diff
)
Cytoskeletal
defects
Microfilaments
Myofilament
Actin
*
Hypertrophic cardiomyopathy 11
Dilated cardiomyopathy 1AA
DFNA20
Nemaline myopathy 3
Myosin
*
Elejalde syndrome
Hypertrophic cardiomyopathy 1, 8, 10
Usher syndrome 1B
Freeman–Sheldon syndrome
DFN A3, 4, 11, 17, 22; B2, 30, 37, 48
May–Hegglin anomaly
Troponin
*
Hypertrophic cardiomyopathy 7, 2
Nemaline myopathy 4, 5
Tropomyosin
*
Hypertrophic cardiomyopathy 3
Nemaline myopathy 1
Other
*
Fibrillin
Marfan syndrome
Weill–Marchesani syndrome
Filamin
FG syndrome 2
Boomerang dysplasia
Larsen syndrome
Terminal osseous dysplasia with pigmentary defects
IF
1/2
*
Keratinopathy
(
keratosis
,
keratoderma
,
hyperkeratosis
):
KRT1
Striate palmoplantar keratoderma 3
Epidermolytic hyperkeratosis
IHCM
KRT2E
(
Ichthyosis bullosa of Siemens
)
KRT3
(
Meesmann juvenile epithelial corneal dystrophy
)
KRT4
(
White sponge nevus
)
KRT5
(
Epidermolysis bullosa simplex
)
KRT8
(
Familial cirrhosis
)
KRT10
(
Epidermolytic hyperkeratosis
)
KRT12
(
Meesmann juvenile epithelial corneal dystrophy
)
KRT13
(
White sponge nevus
)
KRT14
(
Epidermolysis bullosa simplex
)
KRT17
(
Steatocystoma multiplex
)
KRT18
(
Familial cirrhosis
)
KRT81
/
KRT83
/
KRT86
(
Monilethrix
)
Naegeli–Franceschetti–Jadassohn syndrome
Reticular pigmented anomaly of the flexures
3
*
Desmin
:
Desmin-related myofibrillar myopathy
Dilated cardiomyopathy 1I
GFAP
:
Alexander disease
Peripherin
:
Amyotrophic lateral sclerosis
4
*
Neurofilament
:
Parkinson's disease
Charcot–Marie–Tooth disease 1F, 2E
Amyotrophic lateral sclerosis
5
*
Laminopathy
: LMNA
Mandibuloacral dysplasia
Dunnigan
Familial partial lipodystrophy
Emery–Dreifuss muscular dystrophy 2
Limb-girdle muscular dystrophy 1B
Charcot–Marie–Tooth disease 2B1
LMNB
Barraquer–Simons syndrome
LEMD3
Buschke–Ollendorff syndrome
Osteopoikilosis
LBR
Pelger–Huet anomaly
Hydrops-ectopic calcification-moth-eaten skeletal dysplasia
Microtubules
Kinesin
*
Charcot–Marie–Tooth disease 2A
Hereditary spastic paraplegia 10
Dynein
*
Primary ciliary dyskinesia
Short rib-polydactyly syndrome 3
Asphyxiating thoracic dysplasia 3
Other
*
Tauopathy
Cavernous venous malformation
Membrane
*
Spectrin
:
Spinocerebellar ataxia 5
Hereditary spherocytosis 2, 3
Hereditary elliptocytosis 2, 3
Ankyrin
:
Long QT syndrome 4
Hereditary spherocytosis 1
Catenin
*
APC
Gardner's syndrome
Familial adenomatous polyposis
plakoglobin
(
Naxos syndrome
)
GAN
(
Giant axonal neuropathy
)
Related topics:
Cytoskeletal proteins
Categories
:
Cytoskeletal defects
Genetic disease and disorder templates by mechanism
