ODCs

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1 OMIM reference -
3 associated genes
5 signs/symptoms

PROTEIN INTERACTIONS: 1

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

Familial hypofibrinogenemia

Short stature due to partial GHR deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FGB	(0.63)	GHR

Citations in the biomedical literature:

Familial hypofibrinogenemia		Short stature due to partial GHR deficiency
	Synonym(s): (no synonyms)		Synonym(s): - Short stature due to partial growth hormone receptor deficiency

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

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

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

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

Familial hypofibrinogenemia
	Very frequent - Autosomal dominant inheritance - Epistaxis / nose bleeding - Gastrointestinal bleeding / hemorrhage / hematemesis / melena / rectorrhagia - Gingivorrhagia / gingival bleeding - Hemorrhage / hemorrhagic syndrome / excessive / long-lasting bleeding
Short stature due to partial GHR deficiency
(no data available)