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1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 OMIM references -
2 associated genes
15 signs/symptoms
Juvenile polyposis of infancy
Proximal symphalangism

BMPR1A GDF5
PTEN NOG


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
BMPR1A
(0.89)
GDF5



Citations in the biomedical literature:


Juvenile polyposis of infancy
BMPR1A PTEN
Proximal symphalangism
GDF5 NOG



Juvenile polyposis of infancy
Proximal symphalangism

Synonym(s):
- Infantile juvenile polyposis syndrome

Synonym(s):
- Symphalangism, Cushing type

Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease

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

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
1 MeSH reference: C536223

Proximal symphalangism

Very frequent
- Autosomal dominant inheritance
- Camptodactyly of some fingers
- Carpal bones fusion / synostosis
- Symphalangy of fingers
- Tarsal anomaly / fusion / synostosis

Frequent
- Clinodactyly of fingers 1,2,3,4 / overlapping fingers
- Elbow dislocation
- Humeroradial fusion
- Metacarpal anomalies / Archibald's sign
- Sensorineural deafness / hearing loss
- Short hand / brachydactyly

Occasional
- Clinodactyly of fifth finger
- Strabismus / squint
- Syndactyly of fingers / interdigital palm
- Wrist / carpal anomalies


Juvenile polyposis of infancy

(no data available)