ODCs

Click node...

2 OMIM references -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Smith-McCort dysplasia

Multiple keratoacanthoma, Ferguson-Smith type

DYM	(UniProt - OMIM)		TGFBR1	(UniProt - OMIM)
RAB33B	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RAB33B	(0.52)	TGFBR1

Citations in the biomedical literature:

Smith-McCort dysplasia		Multiple keratoacanthoma, Ferguson-Smith type
	Synonym(s): (no synonyms)		Synonym(s): - ESS1 - MSSE - Multiple self-healing squamous epithelioma - Self-healing squamous epithelioma type 1

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

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

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: normal Type of inheritance: autosomal dominant

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.