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Autosomal recessive spastic paraplegia type 30
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Idiopathic central precocious puberty
1 associated gene
No signs/symptoms info
Autosomal recessive spastic paraplegia type 30
Idiopathic central precocious puberty

KIF1A
(UniProt - OMIM)
 MKRN3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
KIF1A
(0.63)
MKRN3


Citations in the biomedical literature:


Autosomal recessive spastic paraplegia type 30
KIF1A
Idiopathic central precocious puberty
MKRN3



Autosomal recessive spastic paraplegia type 30
Idiopathic central precocious puberty

Synonym(s):
- SPG30
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare gynecologic or obstetric 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 recessive
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.