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Atrial septal defect, ostium secundum type
8 OMIM references -
8 associated genes
97 connected diseases
No signs/symptoms info
Disease Type of connection
Tetralogy of Fallot
Familial atrial fibrillation
Single ventricular septal defect
Familial isolated dilated cardiomyopathy
Complete atrioventricular canal - ventricle hypoplasia
46,XY partial gonadal dysgenesis
Thyroid hypoplasia
8p23.1 microdeletion syndrome
Atrial septal defect - atrioventricular conduction defects
Complete atrioventricular canal - Fallot tetralogy
Complete atrioventricular canal - left heart obstruction
Familial isolated congenital asplenia
Familial progressive cardiac conduction defect
Hypoplastic left heart syndrome
Partial atrioventricular canal
Congenital diaphragmatic hernia
Left ventricular noncompaction
Atrial septal defect, ostium primum type
Atrial septal defect, sinus venosus type
Familial sick sinus syndrome
Pancreatic hypoplasia - diabetes - congenital heart disease
Situs inversus totalis
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Familial thoracic aortic aneurysm and aortic dissection
Holt-Oram syndrome
Autosomal dominant Emery-Dreifuss muscular dystrophy
Kabuki syndrome
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Wiskott-Aldrich syndrome
Branchio-oculo-facial syndrome
Char syndrome
Estrogen resistance syndrome
46,XX gonadal dysgenesis
46,XY complete gonadal dysgenesis
Spinocerebellar ataxia type 17
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Benign familial chorea
Brain-lung-thyroid syndrome
Burkitt lymphoma
Papillary or follicular thyroid carcinoma
Precursor T-cell acute lymphoblastic leukemia
Hyperinsulinism due to HNF4A deficiency
MODY syndrome
Aneurysm - osteoarthritis syndrome
Baraitser-Winter syndrome
Developmental malformations - deafness - dystonia
Amyotrophic lateral sclerosis
Autosomal dominant distal renal tubular acidosis
Distal 22q11.2 microdeletion syndrome
Distal renal tubular acidosis with anemia
Hereditary spherocytosis
Hypothyroidism due to deficient transcription factors involved in pituitary development or function
Non-acquired combined pituitary hormone deficiency with spine abnormalities
Southeast Asian ovalocytosis
17q11 microdeletion syndrome
Coffin-Siris syndrome
Familial pancreatic carcinoma
Familial rhabdoid tumor
Frontonasal dysplasia with alopecia and genital anomaly
Generalized juvenile polyposis / juvenile polyposis coli
Hereditary hemorrhagic telangiectasia
Hereditary persistence of fetal hemoglobin - beta-thalassemia
Isolated scaphocephaly
Myhre syndrome
Parietal foramina
Potocki-Shaffer syndrome
Richieri Costa-Pereira syndrome
Weaver syndrome
Becker muscular dystrophy
Duchenne muscular dystrophy
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers
X-linked severe congenital neutropenia
X-linked thrombocytopenia with normal platelets
17q23.1q23.2 microdeletion syndrome
Alobar holoprosencephaly
Lobar holoprosencephaly
Microform holoprosencephaly
Midline interhemispheric variant of holoprosencephaly
Semilobar holoprosencephaly
Septopreoptic holoprosencephaly
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Moyamoya disease
5q14.3 microdeletion syndrome
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Autosomal recessive ataxia, Beauce type
Autosomal recessive myogenic arthrogryposis multiplex congenita
Berardinelli-Seip congenital lipodystrophy
Distal hereditary motor neuropathy type 2
- ASD, ostium secundum type

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

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
(no data available)
External references:
8 OMIM references -
No MeSH references

No signs/symptoms info available.