Protruding tongue
Symptom Information:
Symptom ID: | HPO:0010808 | |||||||||||
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) 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) |
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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) |