Bifid tongue
Symptom Information:
Symptom ID: | HPO:0010297 | |||||||||||
Synonyms: |
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Quality: | ||||||||||||
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 head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Abnormality of the mouth(HPO:0000153) Abnormality of the oral cavity(HPO:0000163) Abnormality of the tongue(HPO:0000157) Bifid tongue(HPO:0010297) MedDRA: |
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Database Frequency: | 17 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Cleft lip/palate - intestinal malrotation - cardiopathy | (Orphanet:2001) |
Deafness-craniofacial syndrome | (Orphanet:3241) |
Diabetic embryopathy | (Orphanet:1926) |
Fraser syndrome | (Orphanet:2052) |
Grix-Blankenship-Peterson syndrome | (Orphanet:2099) |
Holzgreve-Wagner-Rehder syndrome | (Orphanet:2167) |
Joubert syndrome with orofaciodigital defect | (Orphanet:2754) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Orofaciodigital syndrome type 2 | (Orphanet:2751) |
Orofaciodigital syndrome type 3 | (Orphanet:2752) |
Orofaciodigital syndrome type 8 | (Orphanet:2755) |
SHORT RIB-POLYDACTYLY SYNDROME, TYPE IIB | (OMIM:615087) |
Short-rib thoracic dysplasia 3 with or without polydactyly | (OMIM:613091) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Trisomy 8q | (Orphanet:1752) |