Abnormal heart morphology
Symptom Information:
Symptom ID: | HPO:0001627 | ||||||||
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) 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) |