Pulmonic stenosis
Symptom Information:
Symptom ID: | HPO:0001642 | |||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||||||||||||||||||||||
Cross references: |
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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) Pulmonic stenosis(HPO:0001642) MedDRA: Vascular disorders(MedDRA:10047065) Arteriosclerosis, stenosis, vascular insufficiency and necrosis(MedDRA:10003216) Site specific necrosis and vascular insufficiency NEC(MedDRA:10052781) Pulmonic stenosis(HPO:0001642) Cardiac disorders(MedDRA:10007541) Cardiac valve disorders(MedDRA:10046973) Pulmonary valvular disorders(MedDRA:10037445) Pulmonic stenosis(HPO:0001642) |
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Database Frequency: | 89 / 7739 | |||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
3C syndrome | (Orphanet:7) |
ADAMS-OLIVER SYNDROME 1 | (OMIM:100300) |
ADAMS-OLIVER SYNDROME 5 | (OMIM:616028) |
ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY | (OMIM:614262) |
Adams-Oliver syndrome | (Orphanet:974) |
Alström syndrome | (Orphanet:64) |
Aneurysm - osteoarthritis syndrome | (Orphanet:284984) |
Atrial septal defect - atrioventricular conduction defects syndrome | (Orphanet:1479) |
Autosomal recessive infantile hypercalcemia | (Orphanet:300547) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
CARDIOFACIOCUTANEOUS SYNDROME 3 | (OMIM:615279) |
CARDIOFACIOCUTANEOUS SYNDROME 4 | (OMIM:615280) |
CARPENTER SYNDROME 1 | (OMIM:201000) |
CHARGE syndrome | (Orphanet:138) |
CHST3-related skeletal dysplasia | (Orphanet:263463) |
CRANIOACROFACIAL SYNDROME | (OMIM:122850) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cardiomyopathy, dilated, 1S | (OMIM:613426) |
Carpenter syndrome | (Orphanet:65759) |
Cholestasis - pigmentary retinopathy - cleft palate | (Orphanet:1415) |
Chronic atrial and intestinal dysrhythmia syndrome | (Orphanet:435988) |
Congenital heart block | (Orphanet:60041) |
Congenital pulmonary valve stenosis | (Orphanet:3189) |
Costello syndrome | (Orphanet:3071) |
Diabetic embryopathy | (Orphanet:1926) |
Dysmorphism - conductive hearing loss - heart defect | (Orphanet:289553) |
Emanuel syndrome | (Orphanet:96170) |
FRONTOOCULAR SYNDROME | (OMIM:605321) |
Fallot complex - intellectual deficit - growth delay | (Orphanet:3304) |
Familial retinal arterial macroaneurysm | (Orphanet:284247) |
Femoral-facial syndrome | (Orphanet:1988) |
Glaucoma - ectopia - microspherophakia - stiff joints - short stature | (Orphanet:2084) |
HETEROTAXY, VISCERAL, 1, X-LINKED | (OMIM:306955) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Ivemark syndrome | (Orphanet:97548) |
KABUKI SYNDROME 2 | (OMIM:300867) |
KAGAMI-OGATA SYNDROME | (OMIM:608149) |
Keipert syndrome | (Orphanet:2662) |
Keutel syndrome | (Orphanet:85202) |
Koolen-De Vries syndrome | (Orphanet:96169) |
LEOPARD SYNDROME 1 | (OMIM:151100) |
Left ventricular noncompaction 2 | (OMIM:609470) |
MARFANOID HABITUS WITH SITUS INVERSUS | (OMIM:609008) |
MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION | (OMIM:249670) |
MICROPHTHALMIA, SYNDROMIC 9 | (OMIM:601186) |
MUNGAN SYNDROME | (OMIM:611376) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 4 | (OMIM:253800) |
Matthew-Wood syndrome | (Orphanet:2470) |
McDonough syndrome | (Orphanet:2471) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Mowat-Wilson syndrome | (Orphanet:2152) |
NOONAN SYNDROME 1 | (OMIM:163950) |
NOONAN SYNDROME 3 | (OMIM:609942) |
NOONAN SYNDROME 4 | (OMIM:610733) |
NOONAN SYNDROME 6 | (OMIM:613224) |
NOONAN SYNDROME 7 | (OMIM:613706) |
NOONAN SYNDROME 8 | (OMIM:615355) |
Nephronophthisis 16 | (OMIM:615382) |
Nephronophthisis 9 | (OMIM:613824) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome with multiple lentigines | (Orphanet:500) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
PRUNE BELLY SYNDROME WITH PULMONIC STENOSIS, MENTAL RETARDATION, ANDDEAFNESS | (OMIM:264140) |
PULMONIC STENOSIS AND DEAFNESS | (OMIM:178651) |
PULMONIC STENOSIS, ATRIAL SEPTAL DEFECT, AND UNIQUE ELECTROCARDIOGRAPHICABNORMALITIES | (OMIM:178650) |
Pancreatic hypoplasia - diabetes - congenital heart disease | (Orphanet:2255) |
Peters-plus syndrome | (Orphanet:709) |
Pitt-Hopkins-like syndrome 2 | (OMIM:614325) |
Recombinant 8 syndrome | (Orphanet:96167) |
Rhizomelic syndrome, Urbach type | (Orphanet:3098) |
Short stature - valvular heart disease - characteristic facies | (Orphanet:2868) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Supravalvular aortic stenosis | (Orphanet:3193) |
Syndromic diarrhea | (Orphanet:84064) |
TRICHOHEPATOENTERIC SYNDROME 1 | (OMIM:222470) |
VENTRICULAR SEPTAL DEFECT 1 | (OMIM:614429) |
VENTRICULAR SEPTAL DEFECT 3 | (OMIM:614432) |
Ventricular septal defect | (Orphanet:1480) |
WEILL-MARCHESANI SYNDROME 1 | (OMIM:277600) |
WEILL-MARCHESANI SYNDROME 3 | (OMIM:614819) |
Weill-Marchesani syndrome | (Orphanet:3449) |
Werner syndrome | (Orphanet:902) |
Williams syndrome | (Orphanet:904) |
Wolfram syndrome 1 | (OMIM:222300) |
X-linked mandibulofacial dysostosis | (Orphanet:1131) |
[DEL] NEUROFIBROMATOSIS-NOONAN SYNDROME | (OMIM:601321) |