Abnormal heart morphology

Symptom Information:

Symptom ID: HPO:0001627
Synonyms:
Abnormality of the heart [HPO:0001627]
Cardiac abnormality [HPO:0001627]
Cardiac anomalies [HPO:0001627]
Cardiac anomalies [OMIM:Cardiac anomalies]
Cardiac abnormalities [OMIM:Cardiac abnormalities]
Cardiac abnormalities (25 to 35% of patients) [OMIM:Cardiac abnormalities (25 to 35% of patients)]
Cardiac anomalies (13%) [OMIM:Cardiac anomalies (13%)]
Cardiac anomalies (39%) [OMIM:Cardiac anomalies (39%)]
Quality:
Cross references:
OMIM: "Cardiac anomalies" [OMIM:Cardiac anomalies]
OMIM: "Cardiac abnormalities" [OMIM:Cardiac abnormalities]
OMIM: "Cardiac abnormalities (25 to 35% of patients)" [OMIM:Cardiac abnormalities (25 to 35% of patients)]
OMIM: "Cardiac anomalies (13%)" [OMIM:Cardiac anomalies (13%)]
OMIM: "Cardiac anomalies (39%)" [OMIM:Cardiac anomalies (39%)]
Is a (Direct Parents):
HPO         obsolete Abnormal heart morphology
HPO         Abnormality of the cardiovascular system
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormal heart morphology(HPO:0001627)
MedDRA:
Database Frequency: 19 / 7739
Resource:

All diseases associated with this symptom:

Bardet-Biedl syndrome 11 (OMIM:615988)
Bardet-Biedl syndrome 7 (OMIM:615984)
Bardet-Biedl syndrome 9 (OMIM:615986)
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 (Orphanet:231117)
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 (Orphanet:96193)
Congenital lactic acidosis, Saguenay-Lac-St. Jean type (Orphanet:70472)
Craniofaciofrontodigital syndrome (Orphanet:363705)
Diabetic embryopathy (Orphanet:1926)
Fraser syndrome (Orphanet:2052)
Glaucoma - ectopia - microspherophakia - stiff joints - short stature (Orphanet:2084)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
Meckel syndrome, type 4 (OMIM:611134)
Monosomy 18q (Orphanet:1600)
Multifocal atrial tachycardia (Orphanet:3282)
Nephronophthisis 9 (OMIM:613824)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
Orofaciodigital syndrome type 1 (Orphanet:2750)
TRICHOHEPATOENTERIC SYNDROME 2 (OMIM:614602)
WEILL-MARCHESANI SYNDROME 1 (OMIM:277600)