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3 OMIM references -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
6 associated genes
No signs/symptoms info
Homozygous familial hypercholesterolemia
Inflammatory myofibroblastic tumor

APOB ALK
LDLR CARS
LDLRAP1 CLTC
PCSK9 RANBP2
TPM3
TPM4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LDLRAP1
(0.75)
CLTC



Citations in the biomedical literature:


Homozygous familial hypercholesterolemia
APOB LDLR LDLRAP1 PCSK9
Inflammatory myofibroblastic tumor
ALK CARS CLTC RANBP2 TPM3 TPM4



Homozygous familial hypercholesterolemia
Inflammatory myofibroblastic tumor

Synonym(s):
- HoFH

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Inborn errors of metabolism
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare oncologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)

External references:
3 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.