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

Laron syndrome with immunodeficiency

Autosomal dominant Charcot-Marie-Tooth disease type 2N


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	STAT5B	(0.63)	AARS

Citations in the biomedical literature:

Laron syndrome with immunodeficiency		Autosomal dominant Charcot-Marie-Tooth disease type 2N
	Synonym(s): - Laron-like syndrome - Short stature due to STAT5b deficiency		Synonym(s): - CMT2N

	Classification (Orphanet): - Rare endocrine disease - Rare genetic disease - Rare immune disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: - Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable 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.