Abnormality of the cardiac septa
Symptom Information:
Symptom ID: | HPO:0001671 | ||||||||||||||||||||||||||||||||||||||||
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 cardiac septa(HPO:0001671) MedDRA: Cardiac disorders(MedDRA:10007541) Abnormality of the myocardium(HPO:0001637) Myocardial disorders NEC(MedDRA:10028590) Abnormality of the cardiac septa(HPO:0001671) |
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Database Frequency: | 55 / 7739 | ||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
14q11.2 microdeletion syndrome | (Orphanet:261120) |
17q12 microduplication syndrome | (Orphanet:261272) |
ADAMS-OLIVER SYNDROME 4 | (OMIM:615297) |
APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIALDYSMORPHISM, AND OTHER CONGENITAL ANOMALIES | (OMIM:300887) |
ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2 | (OMIM:613404) |
ATTRV122I amyloidosis | (Orphanet:85451) |
Acro-renal-ocular syndrome | (Orphanet:959) |
Acrocallosal syndrome | (Orphanet:36) |
Aldosterone-producing adenoma with seizures and neurological abnormalities | (Orphanet:369929) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
BRACHYDACTYLY, TYPE E, WITH ATRIAL SEPTAL DEFECT, TYPE II | (OMIM:113301) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
CARPENTER SYNDROME 2 | (OMIM:614976) |
CHILD syndrome | (Orphanet:139) |
CHROMOSOME 15q25 DELETION SYNDROME | (OMIM:614294) |
Cardiomyopathy, familial hypertrophic, 13 | (OMIM:613243) |
Cholestasis - pigmentary retinopathy - cleft palate | (Orphanet:1415) |
Congenital heart block | (Orphanet:60041) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Distal monosomy 10q | (Orphanet:96148) |
Distal monosomy 15q | (Orphanet:1596) |
Faisalabad histiocytosis | (Orphanet:254707) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
Floating-Harbor syndrome | (Orphanet:2044) |
H syndrome | (Orphanet:168569) |
HAJDU-CHENEY SYNDROME | (OMIM:102500) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2 | (OMIM:614749) |
Hereditary orotic aciduria | (Orphanet:30) |
Holt-Oram syndrome | (Orphanet:392) |
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency | (Orphanet:401948) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Hypoplastic left heart syndrome | (Orphanet:2248) |
Intellectual deficit, X-linked - craniofacioskeletal syndrome | (Orphanet:163979) |
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome | (Orphanet:363611) |
KABUKI SYNDROME 2 | (OMIM:300867) |
LOEYS-DIETZ SYNDROME 1 | (OMIM:609192) |
LOEYS-DIETZ SYNDROME 2 | (OMIM:610168) |
Lung agenesis - heart defect - thumb anomalies | (Orphanet:1120) |
Meckel syndrome | (Orphanet:564) |
Meckel syndrome, type 1 | (OMIM:249000) |
Methylmalonic acidemia with homocystinuria, type cblJ | (Orphanet:369955) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Myhre syndrome | (Orphanet:2588) |
NOONAN SYNDROME 1 | (OMIM:163950) |
Nephronophthisis 3 | (OMIM:604387) |
Okihiro syndrome | (Orphanet:93293) |
Pigmented hypertrichosis with insulin dependent diabetes mellitus syndrome | (Orphanet:254723) |
Rosaï-Dorfman disease | (Orphanet:158014) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
Thiamine-responsive megaloblastic anemia syndrome | (Orphanet:49827) |
Thrombocytopenia - absent radius | (Orphanet:3320) |
VENTRICULAR SEPTAL DEFECT 1 | (OMIM:614429) |
VENTRICULAR SEPTAL DEFECT 3 | (OMIM:614432) |
VERHEIJ SYNDROME | (OMIM:615583) |
[DEL] ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1 | (OMIM:208085) |