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Self-healing collodion baby

3 OMIM references -
3 associated genes
3 signs/symptoms

PROTEIN INTERACTIONS: 1

Atypical Werner syndrome

1 associated gene
No signs/symptoms info

Self-healing collodion baby

Atypical Werner syndrome

ALOX12B	(UniProt - OMIM)		LMNA	(UniProt - OMIM)
ALOXE3	(UniProt - OMIM)
TGM1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ALOX12B	(0.67)	LMNA

Citations in the biomedical literature:

Self-healing collodion baby		Atypical Werner syndrome
	Synonym(s): - SHCB		Synonym(s): - Atypical progeroid syndrome

	Classification (Orphanet): - Rare genetic disease - Rare skin disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	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: (no data available)

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

Self-healing collodion baby
	Very frequent - Autosomal recessive inheritance - Ichthyosis / ichthyosiform dermatitis - Restricted joint mobility / joint stiffness / ankylosis
Atypical Werner syndrome
(no data available)