Glossoptosis

Symptom Information:

Symptom ID: HPO:0000162
Synonyms:
Glossoptosis (disorder) [Orphanet:10210]
Glossoptosis [Orphanet:10210]
Glossoptosis [OMIM:Glossoptosis]
Glossoptosis [MedDRA:10059138]
Tongue swallowing [MedDRA:10059138]
Glossoptosis (46%) [OMIM:Glossoptosis (46%)]
Quality:
Cross references:
Orphanet:10210 "Glossoptosis" [Orphanet:10210]
OMIM: "Glossoptosis" [OMIM:Glossoptosis]
OMIM: "Glossoptosis (46%)" [OMIM:Glossoptosis (46%)]
UMLS:C0267048 "Glossoptosis" [HPO:0000162]
UMLS:C0267048 "Glossoptosis" [Orphanet:10210]
Is a (Direct Parents):
Orphanet Abnormality of the tongue
HPO         Abnormality of the tongue
MedDRA Respiratory signs and symptoms NEC
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)
                         Glossoptosis(HPO:0000162)
MedDRA:
Respiratory, thoracic and mediastinal disorders(MedDRA:10038738)
    Respiratory disorders NEC(MedDRA:10038716)
       Respiratory signs and symptoms NEC(MedDRA:10027698)
          Glossoptosis(HPO:0000162)
Database Frequency: 26 / 7739
Resource:

All diseases associated with this symptom:

AURICULOCONDYLAR SYNDROME 1 (OMIM:602483)
AURICULOCONDYLAR SYNDROME 2 (OMIM:614669)
AURICULOCONDYLAR SYNDROME 3 (OMIM:615706)
Auriculocondylar syndrome (Orphanet:137888)
CATEL-MANZKE SYNDROME (OMIM:616145)
Carey-Fineman-Ziter syndrome (Orphanet:1358)
Catel-Manzke syndrome (Orphanet:1388)
Cerebro-costo-mandibular syndrome (Orphanet:1393)
Hallermann-Streiff syndrome (Orphanet:2108)
Hepatic fibrosis - renal cysts - intellectual deficit (Orphanet:2031)
Isolated Pierre Robin syndrome (Orphanet:718)
Kniest dysplasia (Orphanet:485)
Marshall-Smith syndrome (Orphanet:561)
Otopalatodigital syndrome type 2 (Orphanet:90652)
Pierre Robin syndrome - faciodigital anomaly (Orphanet:2888)
Richieri Costa-Pereira syndrome (Orphanet:3102)
Robin sequence - oligodactyly (Orphanet:3104)
Sternal malformation - vascular dysplasia (Orphanet:3195)
Stickler syndrome (Orphanet:828)
Stickler syndrome type 3 (Orphanet:166100)
TARP syndrome (Orphanet:2886)
Thrombocytopenia - Robin sequence (Orphanet:3323)
Toriello-Carey syndrome (Orphanet:3338)
Treacher-Collins syndrome (Orphanet:861)
Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence (Orphanet:3201)
Yunis-Varon syndrome (Orphanet:3472)