Abnormality of the heart valves
Symptom Information:
Symptom ID: | HPO:0001654 | |||||||||||||||||
Synonyms: |
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Cross references: |
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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) Abnormal heart morphology(HPO:0001627) obsolete Malformation of the heart and great vessels(HPO:0002564) Abnormality of the heart valves(HPO:0001654) MedDRA: Cardiac disorders(MedDRA:10007541) Cardiac valve disorders(MedDRA:10046973) Cardiac valve disorders NEC(MedDRA:10046971) Abnormality of the heart valves(HPO:0001654) |
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Database Frequency: | 49 / 7739 | |||||||||||||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
3C syndrome | (Orphanet:7) |
Alkaptonuria | (Orphanet:56) |
Autosomal dominant cutis laxa | (Orphanet:90348) |
CHILD syndrome | (Orphanet:139) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cardiomyopathy-cataract-hip spine disease | (Orphanet:1345) |
Chronic atrial and intestinal dysrhythmia syndrome | (Orphanet:435988) |
Cogan syndrome | (Orphanet:1467) |
Cutis laxa | (Orphanet:209) |
Cutis laxa-Marfanoid syndrome | (Orphanet:171719) |
EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED | (OMIM:130090) |
Ehlers-Danlos syndrome type 1 | (Orphanet:90309) |
Ehlers-Danlos syndrome with periventricular heterotopia | (Orphanet:82004) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Ellis Van Creveld syndrome | (Orphanet:289) |
Fabry disease | (Orphanet:324) |
GM1 gangliosidosis | (Orphanet:354) |
GM1 gangliosidosis type 1 | (Orphanet:79255) |
Gaucher disease | (Orphanet:355) |
Gaucher disease - ophthalmoplegia - cardiovascular calcification | (Orphanet:2072) |
Gaucher disease type 3 | (Orphanet:77261) |
Geleophysic dysplasia | (Orphanet:2623) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Kawasaki disease | (Orphanet:2331) |
MUCOPOLYSACCHARIDOSES, UNCLASSIFIED TYPES | (OMIM:252700) |
Mosaic trisomy 9 | (Orphanet:99776) |
Mucolipidosis type 2 | (Orphanet:576) |
Mucolipidosis type 3 | (Orphanet:577) |
Mucopolysaccharidosis type 1 | (Orphanet:579) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Mucopolysaccharidosis type 2, attenuated form | (Orphanet:217093) |
Mucopolysaccharidosis type 4 | (Orphanet:582) |
Mucopolysaccharidosis type 4A | (Orphanet:309297) |
Mucopolysaccharidosis type 6 | (Orphanet:583) |
Mucopolysaccharidosis type 7 | (Orphanet:584) |
Nephronophthisis 12 | (OMIM:613820) |
Nephronophthisis 2 | (OMIM:602088) |
Nephronophthisis 3 | (OMIM:604387) |
Pallister-Hall syndrome | (Orphanet:672) |
Rheumatic fever | (Orphanet:3099) |
Scheie syndrome | (Orphanet:93474) |
Short stature - valvular heart disease - characteristic facies | (Orphanet:2868) |
Sneddon syndrome | (Orphanet:820) |
Takayasu arteritis | (Orphanet:3287) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |