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PROTEIN INTERACTIONS: 2
3 OMIM references -
5 associated genes
No signs/symptoms info
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
Autoimmune lymphoproliferative syndrome

BTK CASP10
ELF4 FAS
FASLG
NRAS
PRKCD


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
BTK
BTK
(0.65)
(0.52)
FASLG
FAS



Citations in the biomedical literature:


Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
BTK ELF4
Autoimmune lymphoproliferative syndrome
CASP10 FAS FASLG NRAS PRKCD



Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
Autoimmune lymphoproliferative syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- ALPS
- Canale-Smith syndrome
- FAS deficiency

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

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

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

External references:
1 OMIM reference -
No MeSH references
External references:
3 OMIM references -
1 MeSH reference: D056735

No signs/symptoms info available.