ODCs

Click node...

4 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
7 signs/symptoms

Pediatric systemic lupus erythematosus

Autosomal recessive limb-girdle muscular dystrophy type 2H


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	IRAK1	(0.68)	TRIM32

Citations in the biomedical literature:

Pediatric systemic lupus erythematosus		Autosomal recessive limb-girdle muscular dystrophy type 2H
	Synonym(s): - SLE, pediatric onset		Synonym(s): - LGMD2H - Limb-girdle muscular dystrophy due to TRIM32 deficiency - Sarcotubular myopathy

	Classification (Orphanet): - Rare neurologic disease - Rare renal disease - Rare respiratory disease - Rare systemic or rheumatologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the musculoskeletal system and connective tissue -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: no data available Type of inheritance: autosomal recessive

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - No MeSH references

Autosomal recessive limb-girdle muscular dystrophy type 2H
	Very frequent - Abnormal EMG / electromyogram / electropmyography - Abnormal gait - Abnormal muscle biopsy / muscle enzymes / CPK / LDH / aldolase / creatin phosphokinase - Autosomal recessive inheritance - Expressionless face / amimia - Myopathy Frequent - Tall stature / gigantism / growth acceleration
Pediatric systemic lupus erythematosus
(no data available)