Abnormality of the pharynx
Symptom Information:
Symptom ID: | HPO:0000600 | ||||||||
Synonyms: |
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Quality: | |||||||||
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 pharynx(HPO:0000600) MedDRA: |
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Database Frequency: | 22 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
17p11.2 microduplication syndrome | (Orphanet:1713) |
22q11.2 deletion syndrome | (Orphanet:567) |
22q11.2 microduplication syndrome | (Orphanet:1727) |
Adducted thumbs - arthrogryposis, Christian type | (Orphanet:2952) |
Charcot-Marie-Tooth disease | (Orphanet:166) |
Congenital velopharyngeal incompetence | (Orphanet:2291) |
Deafness - small bowel diverticulosis - neuropathy | (Orphanet:3217) |
Dyskeratosis congenita | (Orphanet:1775) |
Goldenhar syndrome | (Orphanet:374) |
HEC syndrome | (Orphanet:2119) |
Imperforate oropharynx - costo vetebral anomalies | (Orphanet:2759) |
Infant botulism | (Orphanet:178478) |
Isolated Pierre Robin syndrome | (Orphanet:718) |
Maple syrup urine disease | (Orphanet:511) |
Neuronal intranuclear inclusion disease | (Orphanet:2289) |
Oculopharyngeal muscular dystrophy | (Orphanet:270) |
Omphalocele syndrome, Shprintzen-Goldberg type | (Orphanet:3164) |
Opitz G/BBB syndrome | (Orphanet:2745) |
Oral submucous fibrosis | (Orphanet:357154) |
Primary basilar impression | (Orphanet:2285) |
Schwartz-Jampel syndrome | (Orphanet:800) |
XK aprosencephaly | (Orphanet:3469) |