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Familial atrial myxoma
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Isolated anophthalmia - microphthalmia
7 OMIM references -
7 associated genes
No signs/symptoms info
Familial atrial myxoma
Isolated anophthalmia - microphthalmia

PRKAR1A
(UniProt - OMIM)
 ALDH1A3
(UniProt - OMIM)
GDF3
(UniProt - OMIM)
OTX2
(UniProt - OMIM)
PRSS56
(UniProt - OMIM)
RAX
(UniProt - OMIM)
SOX2
(UniProt - OMIM)
VSX2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PRKAR1A
(0.63)
SOX2


Citations in the biomedical literature:


Familial atrial myxoma
PRKAR1A
Isolated anophthalmia - microphthalmia
ALDH1A3 GDF3 OTX2 PRSS56 RAX SOX2
VSX2



Familial atrial myxoma
Isolated anophthalmia - microphthalmia

Synonym(s):
(no synonyms)

Synonym(s):
- Clinical anophthalmia
- Isolated pure microphthalmia
- Primitive anophthalmia
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare oncologic disease
Classification (Orphanet):
(no data available)
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: C538262
External references:
7 OMIM references -
No MeSH references
No signs/symptoms info available.