Abnormality of the cardiovascular system

Symptom Information:

Symptom ID: HPO:0001626
Synonyms:
Cardiovascular abnormality [HPO:0001626]
Cardiovascular disease [HPO:0001626]
Quality:
Cross references:
Is a (Direct Parents):
HPO         Abnormality of cardiovascular system morphology
HPO         Phenotypic abnormality
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the cardiovascular system(HPO:0001626)
MedDRA:
Database Frequency: 73 / 7739
Resource:

All diseases associated with this symptom:

17p11.2 microduplication syndrome (Orphanet:1713)
ARTERIES, ANOMALIES OF (OMIM:108000)
Acro-renal-mandibular syndrome (Orphanet:958)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Atrophoderma vermiculata (Orphanet:79100)
Autosomal dominant Larsen syndrome (Orphanet:503)
Autosomal recessive cutis laxa type 1 (Orphanet:90349)
Autosomal recessive cutis laxa type 2 (Orphanet:90350)
BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1 (OMIM:601816)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 12 (OMIM:615989)
Bardet-Biedl syndrome 13 (OMIM:615990)
Bardet-Biedl syndrome 6 (OMIM:605231)
Bethlem myopathy (Orphanet:610)
Brachydactyly-long thumb syndrome (Orphanet:2946)
COWDEN SYNDROME 5 (OMIM:615108)
COWDEN SYNDROME 6 (OMIM:615109)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Cholestasis - pigmentary retinopathy - cleft palate (Orphanet:1415)
Cirrhotic cardiomyopathy (Orphanet:57777)
Cocaine embryofetopathy (Orphanet:1911)
Congenital atransferrinemia (Orphanet:1195)
Congenital chloride diarrhea (Orphanet:53689)
Congenital hydronephrosis (Orphanet:2190)
Cowden syndrome (Orphanet:201)
Craniofaciofrontodigital syndrome (Orphanet:363705)
Diabetic embryopathy (Orphanet:1926)
Diffuse cutaneous systemic sclerosis (Orphanet:220393)
Distal monosomy 17q (Orphanet:1597)
ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY (OMIM:600351)
Fetal hydantoin syndrome (Orphanet:1912)
Fucosidosis (Orphanet:349)
Gaucher disease type 1 (Orphanet:77259)
Glycogen storage disease due to muscle glycogen phosphorylase deficiency (Orphanet:368)
HYPOADRENOCORTICISM, FAMILIAL (OMIM:240200)
Heart-hand syndrome type 3 (Orphanet:1342)
Hurler syndrome (Orphanet:93473)
Hypoplasminogenemia (Orphanet:722)
Intellectual deficit, X-linked - psychosis - macroorchidism (Orphanet:3077)
Isolated Dandy-Walker malformation (Orphanet:217)
Isolated polycystic liver disease (Orphanet:2924)
LEG ULCERS, FAMILIAL, OF JUVENILE ONSET (OMIM:150590)
Limb transversal defect - cardiac anomaly (Orphanet:2492)
Limited cutaneous systemic sclerosis (Orphanet:220402)
Limited systemic sclerosis (Orphanet:220407)
MUSCULAR HYPERTONIA, LETHAL (OMIM:254120)
MYOPATHY, MYOSIN STORAGE (OMIM:608358)
Malonic aciduria (Orphanet:943)
Marfanoid habitus - intellectual deficit, autosomal recessive (Orphanet:2463)
Microphthalmia with limb anomalies (Orphanet:1106)
Miller-Dieker syndrome (Orphanet:531)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, attenuated form (Orphanet:217093)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Necrotizing encephalomyelopathy, subacute, of Leigh, adult (OMIM:161700)
Ondine syndrome (Orphanet:661)
PREPAPILLARY VASCULAR LOOPS (OMIM:264060)
Paris-Trousseau thrombocytopenia (Orphanet:851)
Rhombencephalosynapsis (Orphanet:59315)
Roifman syndrome (Orphanet:353298)
Silver-Russell syndrome (Orphanet:813)
Sirenomelia (Orphanet:3169)
Skin fragility-woolly hair-palmoplantar keratoderma syndrome (Orphanet:293165)
Solitary fibrous tumor (Orphanet:2126)
THUMB DEFORMITY (OMIM:188100)
Toriello-Lacassie-Droste syndrome (Orphanet:3339)
VENULAR INSUFFICIENCY, SYSTEMIC (OMIM:192700)
Van Regemorter-Pierquin-Vamos syndrome (Orphanet:3419)
Watson syndrome (Orphanet:3444)
Williams syndrome (Orphanet:904)
X-linked sideroblastic anemia (Orphanet:75563)