ODCs

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3 OMIM references -
3 associated genes
3 signs/symptoms

PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
4 signs/symptoms

Self-healing collodion baby

Localized epidermolysis bullosa simplex


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ALOX12B	(0.65)	KRT5

Citations in the biomedical literature:

Self-healing collodion baby		Localized epidermolysis bullosa simplex
	Synonym(s): - SHCB		Synonym(s): - EBS-loc - Epidermolysis bullosa simplex of palms and soles - Epidermolysis bullosa simplex, Weber-Cockayne type

	Classification (Orphanet): - Rare genetic disease - Rare skin disease		Classification (Orphanet): - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood Average age of death: normal Type of inheritance: autosomal dominant

	External references: 3 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

Self-healing collodion baby		Localized epidermolysis bullosa simplex
	Very frequent - Autosomal recessive inheritance - Ichthyosis / ichthyosiform dermatitis - Restricted joint mobility / joint stiffness / ankylosis		Very frequent - Autosomal dominant inheritance - Ecchymoses - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment Frequent - Hyperhidrosis / increased sweating