Short mandibular rami

Symptom Information:

Symptom ID: HPO:0003778
Synonyms:
Short body and ramus of mandible [HPO:0003778]
Short mandibular ramus [HPO:0003778]
Underdeveloped mandibular rami [HPO:0003778]
Short body and ramus of mandible [OMIM:Short body and ramus of mandible]
Short mandibular rami [OMIM:Short mandibular rami]
Short mandibular ramus [OMIM:Short mandibular ramus]
Underdeveloped mandibular rami [OMIM:Underdeveloped mandibular rami]
Quality:
Cross references:
OMIM: "Short body and ramus of mandible" [OMIM:Short body and ramus of mandible]
OMIM: "Short mandibular rami" [OMIM:Short mandibular rami]
OMIM: "Short mandibular ramus" [OMIM:Short mandibular ramus]
OMIM: "Underdeveloped mandibular rami" [OMIM:Underdeveloped mandibular rami]
Is a (Direct Parents):
HPO         Micrognathia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal axial skeleton morphology(HPO:0009121)
                Aplasia/hypoplasia affecting bones of the axial skeleton(HPO:0009122)
                   Aplasia/Hypoplasia involving bones of the skull(HPO:0009116)
                      Aplasia/Hypoplasia of the mandible(HPO:0009118)
                         Micrognathia(HPO:0000347)
                            Short mandibular rami(HPO:0003778)
                Abnormality of the skull(HPO:0000929)
                   Aplasia/Hypoplasia involving bones of the skull(HPO:0009116)
                      Aplasia/Hypoplasia of the mandible(HPO:0009118)
                         Micrognathia(HPO:0000347)
                            Short mandibular rami(HPO:0003778)
                   Abnormality of facial skeleton(HPO:0011821)
                      Abnormality of the mandible(HPO:0000277)
                         Aplasia/Hypoplasia of the mandible(HPO:0009118)
                            Micrognathia(HPO:0000347)
                               Short mandibular rami(HPO:0003778)
             Aplasia/hypoplasia involving the skeleton(HPO:0009115)
                Aplasia/hypoplasia affecting bones of the axial skeleton(HPO:0009122)
                   Aplasia/Hypoplasia involving bones of the skull(HPO:0009116)
                      Aplasia/Hypoplasia of the mandible(HPO:0009118)
                         Micrognathia(HPO:0000347)
                            Short mandibular rami(HPO:0003778)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the skull(HPO:0000929)
                Aplasia/Hypoplasia involving bones of the skull(HPO:0009116)
                   Aplasia/Hypoplasia of the mandible(HPO:0009118)
                      Micrognathia(HPO:0000347)
                         Short mandibular rami(HPO:0003778)
                Abnormality of facial skeleton(HPO:0011821)
                   Abnormality of the mandible(HPO:0000277)
                      Aplasia/Hypoplasia of the mandible(HPO:0009118)
                         Micrognathia(HPO:0000347)
                            Short mandibular rami(HPO:0003778)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

AURICULOCONDYLAR SYNDROME 1 (OMIM:602483)
AURICULOCONDYLAR SYNDROME 2 (OMIM:614669)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Hurler syndrome (Orphanet:93473)
Marshall-Smith syndrome (Orphanet:561)
Oculoauriculovertebral spectrum with radial defects (Orphanet:2549)
Progressive hemifacial atrophy (Orphanet:1214)