Molar tooth sign on MRI
Symptom Information:
| Symptom ID: | HPO:0002419 | |||||||||
| Synonyms: |
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| Is a (Direct Parents): |
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| Is a (Whole tree): |
HPO:
MedDRA: |
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| Database Frequency: | 27 / 7739 | |||||||||
| Resource: |
All diseases associated with this symptom:
| ARIMA SYNDROME | (OMIM:243910) |
| HYDROLETHALUS SYNDROME 2 | (OMIM:614120) |
| Joubert syndrome | (Orphanet:475) |
| Joubert syndrome 1 | (OMIM:213300) |
| Joubert syndrome 10 | (OMIM:300804) |
| Joubert syndrome 14 | (OMIM:614424) |
| Joubert syndrome 15 | (OMIM:614464) |
| Joubert syndrome 16 | (OMIM:614465) |
| Joubert syndrome 18 | (OMIM:614815) |
| Joubert syndrome 2 | (OMIM:608091) |
| Joubert syndrome 20 | (OMIM:614970) |
| Joubert syndrome 22 | (OMIM:615665) |
| Joubert syndrome 28 | (OMIM:617121) |
| Joubert syndrome 3 | (OMIM:608629) |
| Joubert syndrome 4 | (OMIM:609583) |
| Joubert syndrome 5 | (OMIM:610188) |
| Joubert syndrome 6 | (OMIM:610688) |
| Joubert syndrome 7 | (OMIM:611560) |
| Joubert syndrome 8 | (OMIM:612291) |
| Joubert syndrome 9 | (OMIM:612285) |
| Joubert syndrome with hepatic defect | (Orphanet:1454) |
| Joubert syndrome with ocular defect | (Orphanet:220493) |
| Joubert syndrome with oculorenal defect | (Orphanet:2318) |
| Joubert syndrome with orofaciodigital defect | (Orphanet:2754) |
| Joubert syndrome with renal defect | (Orphanet:220497) |
| Meckel syndrome, type 4 | (OMIM:611134) |
| OROFACIODIGITAL SYNDROME XIV | (OMIM:615948) |