ANXA11 gene related symptoms and diseases

All the information presented here about the ANXA11 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,HGNC,ORPHANET,NCBIGENE, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to ANXA11 gene

Symptoms // Phenotype % Cases
Amyotrophic lateral sclerosis Very Common - Between 80% and 100% cases
Neuronal loss in central nervous system Very Common - Between 80% and 100% cases
Dementia Very Common - Between 80% and 100% cases
Microcephaly Uncommon - Between 30% and 50% cases
Fasciculations Uncommon - Between 30% and 50% cases

Other less frequent symptoms and clinical features

Patients with ANXA11 gene alterations may also develop some of the following symptoms and phenotypes:
  • Not very common - Between 30% and 50% cases

  • Sleep apnea
  • Slurred speech
  • Emotional lability
  • Agitation
  • Bulbar palsy
  • Muscle fibrillation
  • Xerostomia
  • Abnormal lower motor neuron morphology

And 35 more phenotypes, you can get all of them using our tools for rare diseases.

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Rare diseases associated to ANXA11 gene

Here you will find a list of rare diseases related to the ANXA11. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


AMYOTROPHIC LATERAL SCLEROSIS


Alternate names

AMYOTROPHIC LATERAL SCLEROSIS Is also known as als, amyotrophic lateral sclerosis 1, autosomal dominant, fals, lou gehrig disease, charcot disease, amyotrophic lateral sclerosis 1, familial

Description

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive muscular paralysis reflecting degeneration of motor neurons in the primary motor cortex, corticospinal tracts, brainstem and spinal cord.

Most common symptoms of AMYOTROPHIC LATERAL SCLEROSIS

  • Microcephaly
  • Muscle weakness
  • Pain
  • Cataract
  • Spasticity


More info about AMYOTROPHIC LATERAL SCLEROSIS

SOURCES: OMIM MESH ORPHANET

AMYOTROPHIC LATERAL SCLEROSIS 23; ALS23


Most common symptoms of AMYOTROPHIC LATERAL SCLEROSIS 23; ALS23

  • Dementia
  • Pallor
  • Neuronal loss in central nervous system
  • Amyotrophic lateral sclerosis


More info about AMYOTROPHIC LATERAL SCLEROSIS 23; ALS23

SOURCES: OMIM


Potential gene panels for ANXA11 gene

Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Sequencing Panel with CNV Detection Panel

United States.

By PreventionGenetics PreventionGenetics Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Sequencing Panel with CNV Detection that also includes the following genes: SOD1 SQSTM1 TARDBP TBK1 UBQLN2 VAPB VCP OPTN CDH13 TREM2

More info about this panel

Amyotrophic Lateral Sclerosis / Motor Neuron Disease via ANXA11 Gene Sequencing with CNV Detection Panel

United States.

By PreventionGenetics PreventionGenetics

This panel specifically test the ANXA11 gene.

More info about this panel

ANXA11 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the ANXA11 gene.

More info about this panel


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