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1 OMIM reference -
1 associated gene
11 signs/symptoms
COMMON GENES: 1
2 OMIM references -
4 associated genes
No signs/symptoms info
GRACILE syndrome
Leigh syndrome with nephrotic syndrome

BCS1L BCS1L
COQ2
DLD
PDSS2


COMMON
GENES
BCS1L



Citations in the biomedical literature:


GRACILE syndrome
BCS1L
Leigh syndrome with nephrotic syndrome
COQ2 DLD PDSS2



GRACILE syndrome
Leigh syndrome with nephrotic syndrome

Synonym(s):
- Fellman disease
- Growth delay - aminoaciduria - cholestasis - iron overload - lactic acidosis - early death
- Growth restriction - aminoaciduria - cholestasis - iron overload - lactic acidosis - early death

Synonym(s):
- Infantile subacute necrotizing encephalopathy with nephrotic syndrome
- Leigh disease with nephrotic syndrome

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: -
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
1 MeSH reference: C537934
External references:
2 OMIM references -
No MeSH references

GRACILE syndrome

Very frequent
- Aminoacid metabolism anomalies / aminoaciduria
- Autosomal recessive inheritance
- Cirrhosis
- Failure to thrive / difficulties for feeding in infancy / growth delay
- Hearing loss / hypoacusia / deafness
- Hepatitis / icterus / cholestasis
- Hyperferritinemia / iron overload
- Liver / hepatic steatosis
- Renal tubular defect / tubulopathy

Frequent
- Brittle hair / distrix / trichorrhexis
- Early death / lethality



Leigh syndrome with nephrotic syndrome

(no data available)