Cytoscape Web
Click node...

Acral self-healing collodion baby
1 associated gene
1 sign/symptom
PROTEIN INTERACTIONS: 1
Autosomal dominant Charcot-Marie-Tooth disease type 2F
1 OMIM reference -
1 associated gene
No signs/symptoms info
Acral self-healing collodion baby
Autosomal dominant Charcot-Marie-Tooth disease type 2F

TGM1
(UniProt - OMIM)
 HSPB1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
TGM1
(0.55)
HSPB1


Citations in the biomedical literature:


Acral self-healing collodion baby
TGM1
Autosomal dominant Charcot-Marie-Tooth disease type 2F
HSPB1



Acral self-healing collodion baby
Autosomal dominant Charcot-Marie-Tooth disease type 2F

Synonym(s):
- Acral SHCB
Synonym(s):
- CMT2F
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: <1 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
Acral self-healing collodion baby

Very frequent
- Ichthyosis / ichthyosiform dermatitis



Autosomal dominant Charcot-Marie-Tooth disease type 2F

(no data available)