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1 OMIM reference -
1 associated gene
37 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 4
1 OMIM reference -
9 associated genes
13 signs/symptoms
Branchio-oculo-facial syndrome
Tetralogy of Fallot

TFAP2A CITED2
GATA4
GATA5
GATA6
GDF1
GJA5
JAG1
NKX2-5
ZFPM2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TFAP2A
(0.88)
CITED2



Citations in the biomedical literature:


Branchio-oculo-facial syndrome
TFAP2A
Tetralogy of Fallot
CITED2 GATA4 GATA5 GATA6 GDF1 GJA5
JAG1 NKX2-5 ZFPM2



Branchio-oculo-facial syndrome
Tetralogy of Fallot

Synonym(s):
- BOFS

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare maxillo-facial surgical disease
- Rare otorhinolaryngologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare surgical cardiac disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
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: no data available
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: neonatal/infancy
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: D013771


COMMON
SIGNS
- Autosomal dominant inheritance
- Branchial / posterior auricular / preauricular / cheek cysts / fistulae
- Dolichocephaly / scaphocephaly
- Intrauterine growth retardation


Branchio-oculo-facial syndrome
Tetralogy of Fallot

Very frequent
- Capillary hemangioma / nevus / naevus flammeus / port-wine stain
- Conductive deafness / hearing loss
- Dermoid sinus / dimple / pit (excluding sacral)
- External ear anomalies
- Low set ears / posteriorly rotated ears
- Philtrum deeply grooved
- Protruding lips
- Retinoschisis / retinal / chorioretinal coloboma
- Skin hypoplasia / aplasia / atrophy

Frequent
- Abnormal cry / voice / phonation disorder / nasal speech
- Anodontia / oligodontia / hypodontia
- Broad nose / nasal bridge
- Coloboma of iris
- Complete / partial microdontia
- Defect / anomaly of lacrimal system
- Dysplastic / thick / grooved fingernails
- High vaulted / narrow palate
- Lateral cleft lip / gingival cleft / paramedian nasal cleft
- Premature greying of hair
- Short columella / depressed nasal tip
- Short stature / dwarfism / nanism
- Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia
- Upslanted palpebral fissures / mongoloid slanting palpebral fissures

Occasional
- Agenesis / hypoplasia / aplasia of kidneys
- Cataract / lens opacification
- Cleft lip and palate
- Lip pits / fistulae
- Megaureter / hydronephrosis / pyeloureteral junction syndrome
- Microcornea
- Multicystic kidney / renal dysplasia
- Preaxial polydactyly (hand)
- Ptosis
- Strabismus / squint


Very frequent
- Broad forehead
- Clinodactyly of fifth finger
- Long / large / bulbous nose
- Short hand / brachydactyly

Frequent
- Flat supraorbital ridge
- Proptosis / exophthalmos
- Tetralogy of Fallot / trilogy of Fallot
- Thin / retracted lips
- Undescended / ectopic testes / cryptorchidia / unfixed testes