Tongue atrophy
Symptom Information:
Symptom ID: | HPO:0012473 | ||||
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) Tongue atrophy(HPO:0012473) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Tongue conditions(MedDRA:10043946) Tongue disorders(MedDRA:10043954) Tongue atrophy(HPO:0012473) |
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Database Frequency: | 8 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
BROWN-VIALETTO-VAN LAERE SYNDROME 1 | (OMIM:211530) |
Charcot-Marie-Tooth disease type 4C | (Orphanet:99949) |
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1 | (OMIM:158900) |
Facioscapulohumeral dystrophy | (Orphanet:269) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 1B | (OMIM:614678) |
Progressive hemifacial atrophy | (Orphanet:1214) |
Riboflavin transporter deficiency | (Orphanet:97229) |
Spinocerebellar ataxia type 36 | (Orphanet:276198) |