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Ring dermoid of cornea
1 OMIM reference -
1 associated gene
20 connected diseases
No signs/symptoms info
Disease Type of connection
Axenfeld anomaly
Axenfeld-Rieger syndrome
Peters anomaly
Rieger anomaly
Familial atrial fibrillation
Autosomal dominant nonsyndromic intellectual deficit
Craniopharyngioma
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Pilomatrixoma
Athabaskan brainstem dysgenesis syndrome
Bosley-Salih-Alorainy syndrome
Aneurysm - osteoarthritis syndrome
Burkitt lymphoma
Familial thoracic aortic aneurysm and aortic dissection
Precursor T-cell acute lymphoblastic leukemia
Combined pituitary hormone deficiencies, genetic forms
Hypothyroidism due to deficient transcription factors involved in pituitary development or function
Panhypopituitarism
Williams syndrome
Synonym(s):
- Ring dermoid syndrome
Classification (Orphanet):
- Rare eye disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: C535684
Gene symbol UniProt reference OMIM reference
PITX2 Q99697601542
No signs/symptoms info available.