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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
39 signs/symptoms
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Pfeiffer syndrome type 3

APP FGFR2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.56)
FGFR2



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Pfeiffer syndrome type 3
FGFR2



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Pfeiffer syndrome type 3

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

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

Pfeiffer syndrome type 3

Very frequent
- Arnold-Chiari anomaly
- Autosomal dominant inheritance
- Brachycephaly / flat occiput
- Broad / bifid big toe
- Broad / bifid thumb
- Depressed nasal bridge
- External auditory canal atresia / stenosis / agenesis
- High forehead
- High vaulted / narrow palate
- Hypertelorism
- Laryngomalacia
- Mid-facial hypoplasia / short / small midface
- Proptosis / exophthalmos
- Respiratory distress / dyspnea / respiratory failure / lung volume reduction
- Restricted joint mobility / joint stiffness / ankylosis
- Short big toe
- Short / small nose
- Stenosis of aqueduc of Sylvius
- Thumb hypoplasia / aplasia / absence
- Tracheomalacia / tracheobronchomalacia
- Turricephaly / oxycephaly / acrocephaly

Frequent
- Choanal atresia
- Early death / lethality
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Low set ears / posteriorly rotated ears
- Seizures / epilepsy / absences / spasms / status epilepticus
- Short foot / brachydactyly of toes
- Short hand / brachydactyly
- Syndactyly of fingers / interdigital palm
- Syndactyly of toes

Occasional
- Cleft palate without cleft lip / submucosal cleft palate / bifid uvula
- Cranial hypertension
- Ectopic / horseshoe / fused kidneys
- Hearing loss / hypoacusia / deafness
- Imperforate anus / rectum atresia / agenesis / recto-vaginal / vesical / perineal fistula
- Intestinal / gut / bowel malrotation
- Megaureter / hydronephrosis / pyeloureteral junction syndrome
- Vesicorenal / vesicoureteral reflux
- Visual loss / blindness / amblyopia


Hereditary cerebral hemorrhage with amyloidosis, Flemish type

(no data available)