ODCs

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1 associated gene
1 sign/symptom

COMMON GENES: 1
PROTEIN INTERACTIONS: 2
COMMON SIGNS: 1

3 OMIM references -
3 associated genes
3 signs/symptoms

Acral self-healing collodion baby

Self-healing collodion baby


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TGM1 TGM1	(0.49) (0.49)	ALOX12B ALOXE3

Citations in the biomedical literature:

Acral self-healing collodion baby		Self-healing collodion baby
	Synonym(s): - Acral SHCB		Synonym(s): - SHCB

	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: (no data available)		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: No OMIM references No MeSH references		External references: 3 OMIM references - No MeSH references


COMMON SIGNS	- Ichthyosis / ichthyosiform dermatitis

Acral self-healing collodion baby		Self-healing collodion baby
	(no more signs)		Very frequent - Autosomal recessive inheritance - Restricted joint mobility / joint stiffness / ankylosis