Abnormality of the cardiovascular system
Symptom Information:
Symptom ID: | HPO:0001626 | ||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the cardiovascular system(HPO:0001626) MedDRA: |
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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) |