Glossoptosis
Symptom Information:
Symptom ID: | HPO:0000162 | ||||||
Synonyms: |
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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) 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) |
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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) |