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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 OMIM references -
2 associated genes
10 signs/symptoms
Autosomal dominant spastic paraplegia type 13
Isolated 3-methylcrotonyl-CoA carboxylase deficiency

HSPD1 MCCC1
MCCC2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HSPD1
(0.49)
MCCC2



Citations in the biomedical literature:


Autosomal dominant spastic paraplegia type 13
HSPD1
Isolated 3-methylcrotonyl-CoA carboxylase deficiency
MCCC1 MCCC2



Autosomal dominant spastic paraplegia type 13
Isolated 3-methylcrotonyl-CoA carboxylase deficiency

Synonym(s):
- SPG13

Synonym(s):
- 3-methylcrotonylglycinuria
- MCC deficiency
- MCCD

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

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

External references:
1 OMIM reference -
1 MeSH reference: C537485
External references:
2 OMIM references -
1 MeSH reference: C535308

Isolated 3-methylcrotonyl-CoA carboxylase deficiency

Very frequent
- Hypoglycemia
- Hypotonia
- Metabolic anomalies
- Organic acid metabolism anomalies

Frequent
- Failure to thrive / difficulties for feeding in infancy / growth delay
- Hyperammonemia
- Movement disorder

Occasional
- Cerebral vascular anomalies
- Hypertonia / spasticity / rigidity / stiffness
- Respiratory distress / dyspnea / respiratory failure / lung volume reduction


Autosomal dominant spastic paraplegia type 13

(no data available)