Abnormality of cardiovascular system physiology
Symptom Information:
Symptom ID: | HPO:0011025 | ||||
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) Abnormality of cardiovascular system physiology(HPO:0011025) MedDRA: |
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Database Frequency: | 41 / 7739 | ||||
Resource: |
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) |