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1 OMIM reference -
2 associated genes
45 signs/symptoms
PROTEIN INTERACTIONS: 1
14 OMIM references -
17 associated genes
No signs/symptoms info
17q23.1q23.2 microdeletion syndrome
Familial atrial fibrillation

TBX2 ABCC9
TBX4 GATA4
GATA5
GATA6
GJA5
KCNA5
KCNE1
KCNE2
KCNJ2
KCNQ1
NKX2-5
NPPA
NUP155
PITX2
SCN1B
SCN2B
SCN5A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TBX2
(0.59)
NKX2-5



Citations in the biomedical literature:


17q23.1q23.2 microdeletion syndrome
TBX2 TBX4
Familial atrial fibrillation
ABCC9 GATA4 GATA5 GATA6 GJA5 KCNA5
KCNE1 KCNE2 KCNJ2 KCNQ1 NKX2-5 NPPA
NUP155 PITX2 SCN1B SCN2B SCN5A



17q23.1q23.2 microdeletion syndrome
Familial atrial fibrillation

Synonym(s):
- 17q23.1-q23.2 microdeletion syndrome
- Del(17)(q23.1q23.2)
- Monosomy 17q23.1-q23.2
- Monosomy 17q23.1q23.2

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the circulatory system -

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

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

17q23.1q23.2 microdeletion syndrome

Very frequent
- Insterstitial / subtelomeric microdeletion / deletion
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Long foot / arachnodactyly of toes
- Long hand / arachnodactyly

Frequent
- Frontal bossing / prominent forehead
- Intrauterine growth retardation
- Microcephaly
- Patent ductus arteriosus
- Pulmonary hypertension
- Short stature / dwarfism / nanism
- Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia

Occasional
- Abnormal dentition / dental position / implantation / unerupted / dental ankylosis
- Atrial septal defect / interauricular communication
- Bifid tip / cleft nose / supernumerary nose
- Blepharitis / eyelid inflammation
- Chronic / relapsing otitis
- Clinodactyly of fifth finger
- Depressed nasal bridge
- Epicanthic folds
- Epiphyseal anomaly
- Failure to thrive / difficulties for feeding in infancy / growth delay
- Flat foot
- Flexion deformity of toes (excluding big toe) / hammer toe / camptodactyly of toes
- Gastroesophageal reflux / pyrosis / esophagitis / hiatal hernia / gastroparesia
- Hearing loss / hypoacusia / deafness
- High arched eyebrows
- Hip dislocation / dysplasia / coxa valga / coxa vara / coxa plana
- Hypereflexia
- Hypertelorism
- Hypotonia
- Long / large / bulbous nose
- Long / thick / curved lashes / trichomegaly / polytrichia
- Low set ears / posteriorly rotated ears
- Microstomia / little mouth
- Mid-facial hypoplasia / short / small midface
- Patella absent / abnormal (excluding luxation)
- Psychic / behavioural troubles
- Respiratory distress / dyspnea / respiratory failure / lung volume reduction
- Restricted joint mobility / joint stiffness / ankylosis
- Sacral sinus / dimple
- Scoliosis
- Shawl scrotum
- Simian crease / transverse / unique palmar crease
- Strabismus / squint
- Wide space between 1st-2nd toes


Familial atrial fibrillation

(no data available)