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Acral self-healing collodion baby
1 associated gene
1 sign/symptom
PROTEIN INTERACTIONS: 1
Parkinsonian-pyramidal syndrome
2 OMIM references -
2 associated genes
No signs/symptoms info
Acral self-healing collodion baby
Parkinsonian-pyramidal syndrome

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

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


Citations in the biomedical literature:


Acral self-healing collodion baby
TGM1
Parkinsonian-pyramidal syndrome
FBXO7 SNCA



Acral self-healing collodion baby
Parkinsonian-pyramidal syndrome

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

Very frequent
- Ichthyosis / ichthyosiform dermatitis



Parkinsonian-pyramidal syndrome

(no data available)