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Parkinsonian-pyramidal syndrome
2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Self-healing collodion baby
3 OMIM references -
3 associated genes
3 signs/symptoms
Parkinsonian-pyramidal syndrome
Self-healing collodion baby

FBXO7
(UniProt - OMIM)
 ALOX12B
(UniProt - OMIM)
SNCA
(UniProt - OMIM)
 ALOXE3
(UniProt - OMIM)
TGM1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SNCA
(0.52)
TGM1


Citations in the biomedical literature:


Parkinsonian-pyramidal syndrome
FBXO7 SNCA
Self-healing collodion baby
ALOX12B ALOXE3 TGM1



Parkinsonian-pyramidal syndrome
Self-healing collodion baby

Synonym(s):
- Pallidopyramidal syndrome
Synonym(s):
- SHCB
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare skin disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: -
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
2 OMIM references -
No MeSH references
External references:
3 OMIM references -
No MeSH references
Self-healing collodion baby

Very frequent
- Autosomal recessive inheritance
- Ichthyosis / ichthyosiform dermatitis
- Restricted joint mobility / joint stiffness / ankylosis



Parkinsonian-pyramidal syndrome

(no data available)