Abnormality of the pulmonary valve
Symptom Information:
Symptom ID: | HPO:0001641 | ||||||||||
Synonyms: |
|
||||||||||
Quality: | |||||||||||
Cross references: |
|
||||||||||
Is a (Direct Parents): |
|
||||||||||
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) Abnormality of the pulmonary valve(HPO:0001641) MedDRA: Cardiac disorders(MedDRA:10007541) Cardiac valve disorders(MedDRA:10046973) Pulmonary valvular disorders(MedDRA:10037445) Abnormality of the pulmonary valve(HPO:0001641) |
||||||||||
Database Frequency: | 27 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
10q22.3q23.3 microdeletion syndrome | (Orphanet:276413) |
22q11.2 deletion syndrome | (Orphanet:567) |
8p23.1 microduplication syndrome | (Orphanet:251076) |
Adams-Oliver syndrome | (Orphanet:974) |
Aminopterin/methotrexate embryofetopathy | (Orphanet:1908) |
Autosomal dominant cutis laxa | (Orphanet:90348) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Autosomal recessive malignant osteopetrosis | (Orphanet:667) |
Brittle cornea syndrome | (Orphanet:90354) |
Chronic atrial and intestinal dysrhythmia syndrome | (Orphanet:435988) |
Congenital alveolar capillary dysplasia | (Orphanet:210122) |
Costello syndrome | (Orphanet:3071) |
Criss-cross heart | (Orphanet:1461) |
Distal monosomy 19p13.3 | (Orphanet:96129) |
Ehlers-Danlos syndrome, progeroid type | (Orphanet:75496) |
Holoprosencephaly | (Orphanet:2162) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Neurofibromatosis - Noonan syndrome | (Orphanet:638) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome with multiple lentigines | (Orphanet:500) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Osteopetrosis | (Orphanet:2781) |
Polyvalvular heart disease syndrome | (Orphanet:228410) |
Townes-Brocks syndrome | (Orphanet:857) |
Weill-Marchesani syndrome | (Orphanet:3449) |
X-linked mandibulofacial dysostosis | (Orphanet:1131) |
Zunich-Kaye syndrome | (Orphanet:3474) |