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Neurodegeneration with brain iron accumulation due to C19orf12 mutation
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Autosomal recessive spastic paraplegia type 43
1 OMIM reference -
1 associated gene
No signs/symptoms info
Neurodegeneration with brain iron accumulation due to C19orf12 mutation
Autosomal recessive spastic paraplegia type 43

C19ORF12
(UniProt - OMIM)
 C19ORF12
(UniProt - OMIM)

COMMON
GENES 		C19ORF12


Citations in the biomedical literature:


Neurodegeneration with brain iron accumulation due to C19orf12 mutation
C19ORF12
Autosomal recessive spastic paraplegia type 43



Neurodegeneration with brain iron accumulation due to C19orf12 mutation
Autosomal recessive spastic paraplegia type 43

Synonym(s):
- MPAN
- Mitochondrial membrane protein associated neurodegeneration
- NBIA due to C19orf12 mutation
- NBIA5
- Neurodegeneration with brain iron accumulation type 5
Synonym(s):
- SPG43
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.