Furrowed tongue

Symptom Information:

Symptom ID: HPO:0000221
Synonyms:
Prominent tongue grooves [HPO:0000221]
Scrotal tongue [HPO:0000221]
Plicated tongue (disorder) [Orphanet:10350]
Fissured tongue [Orphanet:10350]
Scrotal tongue [OMIM:Scrotal tongue]
Fissured/scrotal tongue [Orphanet:10350]
Plicated tongue [Orphanet:10350]
Plicated tongue [MedDRA:10035630]
Fissured tongue [MedDRA:10035630]
Scrotal tongue [MedDRA:10035630]
Fissured tongue [OMIM:Fissured tongue]
Scrotal tongue (in some patients) [OMIM:Scrotal tongue (in some patients)]
Quality:
Cross references:
Orphanet:10350 "Fissured/scrotal tongue" [Orphanet:10350]
OMIM: "Scrotal tongue" [OMIM:Scrotal tongue]
OMIM: "Fissured tongue" [OMIM:Fissured tongue]
OMIM: "Scrotal tongue (in some patients)" [OMIM:Scrotal tongue (in some patients)]
UMLS:C0040412 "Fissured tongue" [Orphanet:10350]
Is a (Direct Parents):
Orphanet Abnormality of the tongue
MedDRA Tongue disorders
HPO         Abnormality of the tongue
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)
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)