ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
4 signs/symptoms

Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency

Camptodactyly - tall stature - scoliosis - hearing loss


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SH2B1	(0.77)	FGFR3

Citations in the biomedical literature:

Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency		Camptodactyly - tall stature - scoliosis - hearing loss
	Synonym(s): (no synonyms)		Synonym(s): - CATSHL syndrome

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

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

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

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

Camptodactyly - tall stature - scoliosis - hearing loss
	Very frequent - Camptodactyly of fingers - Hearing loss / hypoacusia / deafness - Scoliosis - Tall stature / gigantism / growth acceleration
Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency
(no data available)