Bifid tongue

Symptom Information:

Symptom ID: HPO:0010297
Synonyms:
Split tongue [HPO:0010297]
Bifid tongue (disorder) [Orphanet:10280]
Cleft tongue (disorder) [Orphanet:10280]
Cleft tongue [Orphanet:10280]
Bifid tongue [Orphanet:10280]
Bifid tongue [OMIM:Bifid tongue]
Cleft/notched/bifid tongue [Orphanet:10280]
Bifid tongue (30-45%) [OMIM:Bifid tongue (30-45%)]
Bifid tongue (39%) [OMIM:Bifid tongue (39%)]
Bifid tongue (59%) [OMIM:Bifid tongue (59%)]
Cleft tongue [OMIM:Cleft tongue]
Quality:
Cross references:
Orphanet:10280 "Cleft/notched/bifid tongue" [Orphanet:10280]
OMIM: "Bifid tongue" [OMIM:Bifid tongue]
OMIM: "Bifid tongue (30-45%)" [OMIM:Bifid tongue (30-45%)]
OMIM: "Bifid tongue (39%)" [OMIM:Bifid tongue (39%)]
OMIM: "Bifid tongue (59%)" [OMIM:Bifid tongue (59%)]
OMIM: "Cleft tongue" [OMIM:Cleft tongue]
UMLS:C0431560 "Cleft tongue" [Orphanet:10280]
UMLS:C0266111 "Bifid tongue" [Orphanet:10280]
Is a (Direct Parents):
Orphanet Abnormality of the tongue
HPO         Abnormality of the tongue
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:
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)