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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 OMIM references -
3 associated genes
25 signs/symptoms
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Isolated Klippel-Feil syndrome

APP GDF3
GDF6
MEOX1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.56)
MEOX1



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP
Isolated Klippel-Feil syndrome
GDF3 GDF6 MEOX1



Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Isolated Klippel-Feil syndrome

Synonym(s):
- HCHWA, Flemish type

Synonym(s):
- Congenital cervical vertebral fusion
- Congenital fused cervical segments
- Klippel-Feil malformation
- Klippel-Feil sequence

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

Classification (ICD10):
(no data available)
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 -
No MeSH references
External references:
3 OMIM references -
No MeSH references

Isolated Klippel-Feil syndrome

Very frequent
- Anomalies of spine, vertebrae and pelvis
- Autosomal dominant inheritance
- Autosomal recessive inheritance
- Facial structural asymmetry / facial hemiatrophy / facial hemihypertrophy
- Low hair line (back)
- Short neck
- Vertebral segmentation anomaly / hemivertebrae
- Webbed neck / pterygium colli

Frequent
- Anomalies of the ribs
- Congenital torticolli
- Hearing loss / hypoacusia / deafness
- Narrow / sloping shoulders
- Scapula structural / position anomaly / congenital elevation / Sprengel anomaly
- Scoliosis

Occasional
- Agenesis / hypoplasia / aplasia of kidneys
- Anus ectopia / anteposition / malposition
- Cleft palate without cleft lip / submucosal cleft palate / bifid uvula
- Congenital cardiac anomaly / malformation / cardiopathy
- Cranial nerve anomalies
- Hemiplegia / diplegia / hemiparesia / limb palsy
- Imperforate anus / rectum atresia / agenesis / recto-vaginal / vesical / perineal fistula
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Sacro-coccyx / sacrum anomaly
- Spina bifida
- Ventricular septal defect / interventricular communication


Hereditary cerebral hemorrhage with amyloidosis, Flemish type

(no data available)