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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
7 OMIM references -
5 associated genes
No signs/symptoms info
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Posterior polar cataract

CBL CHMP4B
CRYAB
EPHA2
GJA3
PITX3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CBL
(0.76)
EPHA2



Citations in the biomedical literature:


Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
CBL
Posterior polar cataract
CHMP4B CRYAB EPHA2 GJA3 PITX3



Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Posterior polar cataract

Synonym(s):
- CBL syndrome
- Noonan syndrome-like disorder with JMML

Synonym(s):
- Posterior subcapsular cataract

Classification (Orphanet):
- Rare cardiac disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

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

No signs/symptoms info available.