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Acute infantile liver failure-multisystemic involvement syndrome
2 OMIM references -
2 associated genes
34 connected diseases
No signs/symptoms info
Disease Type of connection
Anaplastic ependymoma
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Hypohidrotic ectodermal dysplasia with immunodeficiency
Incontinentia pigmenti
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Pelizaeus-Merzbacher-like due to AIMP1 mutation
Fibronectin glomerulopathy
Pseudohypoaldosteronism type 2E
Hypomyelination with brain stem and spinal cord involvement and leg spasticity
Autosomal recessive intermediate Charcot-Marie-Tooth disease type B
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Burkitt lymphoma
Precursor T-cell acute lymphoblastic leukemia
46,XY complete gonadal dysgenesis
46,XY partial gonadal dysgenesis
Common variable immunodeficiency
Alveolar soft-part sarcoma
Amish nemaline myopathy
Amyotrophic lateral sclerosis
Autosomal dominant hypohidrotic ectodermal dysplasia
Frontotemporal dementia with motor neuron disease
Giant cell glioblastoma
Glycogen storage disease due to liver phosphorylase kinase deficiency
Juvenile amyotrophic lateral sclerosis
Myxoid / round cell liposarcoma
Translocation renal cell carcinoma
X-linked intellectual deficit, Najm type
Autosomal dominant Charcot-Marie-Tooth disease type 2N
Dedifferentiated liposarcoma
Ketoacidosis due to beta-ketothiolase deficiency
Well-differentiated liposarcoma
X-linked distal arthrogryposis multiplex congenita
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare hepatic disease

Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
2 OMIM references -
No MeSH references

Gene symbol UniProt reference OMIM reference
LARS Q9P2J5151350
MARS P56192156560
No signs/symptoms info available.