Furrowed tongue
Symptom Information:
Symptom ID: | HPO:0000221 | ||||||||||||
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) Furrowed tongue(HPO:0000221) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Tongue conditions(MedDRA:10043946) Tongue disorders(MedDRA:10043954) Furrowed tongue(HPO:0000221) |
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Database Frequency: | 24 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
Acrodermatitis enteropathica, zinc deficiency type | (Orphanet:37) |
COWDEN SYNDROME 5 | (OMIM:615108) |
COWDEN SYNDROME 6 | (OMIM:615109) |
Cataract - intellectual deficit - hypogonadism | (Orphanet:1387) |
Cowden syndrome | (Orphanet:201) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
Distal arthrogryposis type 5D | (Orphanet:329457) |
Dystrophic epidermolysis bullosa | (Orphanet:303) |
Epidermolysis bullosa simplex due to plakophilin deficiency | (Orphanet:158668) |
GEOGRAPHIC TONGUE AND FISSURED TONGUEGLOSSITIS, BENIGN MIGRATORY, INCLUDED | (OMIM:137400) |
Generalized pustular psoriasis | (Orphanet:247353) |
Hereditary mucoepithelial dysplasia | (Orphanet:1839) |
KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT | (OMIM:148210) |
KID syndrome | (Orphanet:477) |
Lhermitte-Duclos disease | (Orphanet:65285) |
Meckel syndrome | (Orphanet:564) |
Melkersson-Rosenthal syndrome | (Orphanet:2483) |
Ophthalmoplegia - intellectual deficit - lingua scrotalis | (Orphanet:2743) |
PACHYONYCHIA CONGENITA 3 | (OMIM:615726) |
Polyneuropathy - intellectual deficit - acromicria - premature menopause | (Orphanet:2928) |
Proteus-like syndrome | (Orphanet:2969) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Syndromic X-linked intellectual deficit due to JARID1C mutation | (Orphanet:85279) |
Zimmermann-Laband syndrome | (Orphanet:3473) |