ODCs

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

PROTEIN INTERACTIONS: 1

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

Diffuse palmoplantar keratoderma with painful fissures

Isolated growth hormone deficiency type II


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	DSG1	(0.63)	GH1

Citations in the biomedical literature:

Diffuse palmoplantar keratoderma with painful fissures		Isolated growth hormone deficiency type II
	Synonym(s): (no synonyms)		Synonym(s): - Congenital IGHD type II - Congenital isolated GH deficiency type II - Congenital isolated growth hormone deficiency type II

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

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

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.