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2 OMIM references -
2 associated genes
8 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 4
1 OMIM reference -
1 associated gene
24 signs/symptoms
Hypoplastic left heart syndrome
Holt-Oram syndrome

GJA1 TBX5
NKX2-5


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NKX2-5
(0.89)
TBX5



Citations in the biomedical literature:


Hypoplastic left heart syndrome
GJA1 NKX2-5
Holt-Oram syndrome
TBX5



Hypoplastic left heart syndrome
Holt-Oram syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- Atriodigital dysplasia type 1
- HOS
- Heart-hand syndrome type 1

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare surgical cardiac disease
Classification (Orphanet):
- Rare bone disease
- Rare cardiac disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- 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: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: unknown
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant

External references:
2 OMIM references -
1 MeSH reference: D018636
External references:
1 OMIM reference -
1 MeSH reference: C535326


COMMON
SIGNS
- Atrial septal defect / interauricular communication
- Hypoplastic aorta / coarctation / stenosis / anomaly / aortic arch interruption
- Hypoplastic left heart / ventricle
- Patent ductus arteriosus


Hypoplastic left heart syndrome
Holt-Oram syndrome

Very frequent
- Stillbirth / neonatal death

Occasional
- Maternal diabetes
- Mitral valve prolapse / incompetence / insufficiency / regurgitation / ring anomaly
- Total / partial trisomy / duplication


Very frequent
- Autosomal dominant inheritance
- Wrist / carpal anomalies

Frequent
- Cardiac conduction defect / sinoauricular / heart / auriculoventricular / branch block
- Fingerlike / triphalangeal thumb
- Metacarpal anomalies / Archibald's sign
- Radius anomaly / absence / agenesis / hypoplasia / abnormal radial ray
- Thumb hypoplasia / aplasia / absence
- Ventricular septal defect / interventricular communication

Occasional
- Anomalies of the ribs
- Anomalous pulmonary venous return
- Atrioventricular canal
- Broad / bifid thumb
- Humerus anomaly / absence / agenesis / hypoplasia / congenital humerus varus
- Narrow / sloping shoulders
- Pectus excavatum
- Phocomelia
- Radioulnar synostosis
- Scapula structural / position anomaly / congenital elevation / Sprengel anomaly
- Scoliosis
- Syndactyly of fingers / interdigital palm