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1 OMIM reference -
5 associated genes
7 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Ondine syndrome
Multiple endocrine neoplasia type 2B

ASCL1 RET
BDNF
EDN3
GDNF
PHOX2B


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
GDNF
(0.52)
RET



Citations in the biomedical literature:


Ondine syndrome
ASCL1 BDNF EDN3 GDNF PHOX2B
Multiple endocrine neoplasia type 2B
RET



Ondine syndrome
Multiple endocrine neoplasia type 2B

Synonym(s):
- CCHS
- Central congenital hypoventilation syndrome
- Congenital central alveolar hypoventilation syndrome
- Ondine curse

Synonym(s):
- MEN2B
- Multiple endocrine neoplasia type 3
- Wagenmann-Froboese syndrome

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D018814

Ondine syndrome

Very frequent
- Dolichocolon / megacolon / megadolichocolon / Hirschsprung's disease
- Respiratory distress / dyspnea / respiratory failure / lung volume reduction

Frequent
- Stillbirth / neonatal death

Occasional
- Central nervous system / peripheral nerves neoplasm / tumor / carcinoma / cancer
- Hypotonia
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Seizures / epilepsy / absences / spasms / status epilepticus


Multiple endocrine neoplasia type 2B

(no data available)