Protruding tongue

Symptom Information:

Symptom ID: HPO:0010808
Synonyms:
Tongue protrusion [HPO:0010808]
Protrusion of tongue [HPO:0010808]
Protrusion of tongue (observable entity) [Orphanet:10070]
Does protrude tongue (finding) [Orphanet:10070]
Does protrude tongue [Orphanet:10070]
Protrusion of tongue [Orphanet:10070]
Protruding tongue [OMIM:Protruding tongue]
Tongue protrusion [OMIM:Tongue protrusion]
Macroglossia/tongue protrusion/proeminent/hypertrophic [Orphanet:10070]
Protrusion tongue [Orphanet:10070]
Protrusion tongue [MedDRA:10037076]
Quality:
Cross references:
Orphanet:10070 "Macroglossia/tongue protrusion/proeminent/hypertrophic" [Orphanet:10070]
OMIM: "Protruding tongue" [OMIM:Protruding tongue]
OMIM: "Tongue protrusion" [OMIM:Tongue protrusion]
UMLS:C0563387 "Does protrude tongue" [Orphanet:10070]
UMLS:C0241442 "Protrusion of tongue" [Orphanet:10070]
Is a (Direct Parents):
Orphanet Abnormality of the tongue
HPO         Abnormality of the tongue
Orphanet Macroglossia
MedDRA Neurological 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)
                         Protruding tongue(HPO:0010808)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Neurological disorders NEC(MedDRA:10029305)
       Neurological signs and symptoms NEC(MedDRA:10029306)
          Protruding tongue(HPO:0010808)
Database Frequency: 28 / 7739
Resource:

All diseases associated with this symptom:

Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 (Orphanet:98791)
Angelman syndrome (Orphanet:72)
COCOON SYNDROME (OMIM:613630)
Carpenter-Waziri syndrome (Orphanet:93973)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Down syndrome (Orphanet:870)
FACIAL ABNORMALITIES, KYPHOSCOLIOSIS, AND MENTAL RETARDATION (OMIM:227250)
Glycogen storage disease due to acid maltase deficiency (Orphanet:365)
Holmes-Gang syndrome (Orphanet:93970)
Hurler syndrome (Orphanet:93473)
ICF syndrome (Orphanet:2268)
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME1 (OMIM:242860)
Joubert syndrome (Orphanet:475)
Joubert syndrome 1 (OMIM:213300)
Juberg-Marsidi syndrome (Orphanet:93972)
Kleefstra syndrome (Orphanet:261494)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
Lethal polymalformative syndrome, Boissel type (Orphanet:210144)
MGAT2-CDG (Orphanet:79329)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) (OMIM:214100)
Pitt-Hopkins-like syndrome 2 (OMIM:614325)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
Smith-Fineman-Myers syndrome (Orphanet:93974)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)
Zellweger syndrome (Orphanet:912)