Abnormality of cardiovascular system physiology

Symptom Information:

Symptom ID: HPO:0011025
Cardiovascular system functional anomaly [Orphanet:35000]
Functional anomalies of the cardio-circulatory system [Orphanet:35000]
Cross references:
Orphanet:35000 "Functional anomalies of the cardio-circulatory system" [Orphanet:35000]
Is a (Direct Parents):
HPO         Cardiogenic shock
HPO         Abnormality of the cardiovascular system
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of cardiovascular system physiology(HPO:0011025)
Database Frequency: 41 / 7739

All diseases associated with this symptom:

20p12.3 microdeletion syndrome (Orphanet:261295)
Aniridia - ptosis - intellectual deficit - familial obesity (Orphanet:1067)
Atrial septal defect - atrioventricular conduction defects syndrome (Orphanet:1479)
Cardiomyopathy, familial restrictive, 1 (OMIM:115210)
Cartilage-hair hypoplasia (Orphanet:175)
Centronuclear myopathy (Orphanet:595)
Cogan syndrome (Orphanet:1467)
Ebstein malformation (Orphanet:1880)
Emery-Dreifuss muscular dystrophy (Orphanet:261)
Endomyocardial fibroelastosis (Orphanet:2022)
Extrasystoles - short stature - hyperpigmentation - microcephaly (Orphanet:1964)
Fabry disease (Orphanet:324)
Familial isolated hypertrophic cardiomyopathy (Orphanet:155)
Familial long QT syndrome (Orphanet:768)
Friedreich ataxia 1 (OMIM:229300)
HEC syndrome (Orphanet:2119)
Heart-hand syndrome type 3 (Orphanet:1342)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Heritable pulmonary arterial hypertension (Orphanet:275777)
Holt-Oram syndrome (Orphanet:392)
IVIC syndrome (Orphanet:2307)
Idiopathic pulmonary arterial hypertension (Orphanet:275766)
Infantile symmetrical thalamic degeneration (Orphanet:3311)
Juvenile dermatomyositis (Orphanet:93672)
Lethal Kniest-like dysplasia (Orphanet:2347)
Lyme disease (Orphanet:91546)
Multifocal muscular fibrosis - obstructed vessels (Orphanet:2033)
Nakajo-Nishimura syndrome (Orphanet:2615)
Noonan syndrome with multiple lentigines (Orphanet:500)
Phocomelia - ectrodactyly - deafness - sinus arrhythmia (Orphanet:2878)
Phosphoribosylpyrophosphate synthetase superactivity (Orphanet:3222)
Polymyositis (Orphanet:732)
Refsum disease (Orphanet:773)
Retinohepatoendocrinologic syndrome (Orphanet:3087)
Scleroderma (Orphanet:801)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Spondylometaphyseal dysplasia, Sedaghatian type (Orphanet:93317)
Torticollis - keloids - cryptorchidism - renal dysplasia (Orphanet:3341)
Ulnar-mammary syndrome (Orphanet:3138)
Usher syndrome (Orphanet:886)
X-linked centronuclear myopathy (Orphanet:596)