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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Distal 17p13.3 microdeletion syndrome
Postaxial polydactyly type A, unilateral

YWHAE GLI3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
YWHAE
(0.63)
GLI3



Citations in the biomedical literature:


Distal 17p13.3 microdeletion syndrome
YWHAE
Postaxial polydactyly type A, unilateral
GLI3



Distal 17p13.3 microdeletion syndrome
Postaxial polydactyly type A, unilateral

Synonym(s):
- Distal del(17)(p13.3 )
- Distal monosomy 17p13.3

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- 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:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.