Palmoplantar keratoderma

Symptom Information:

Symptom ID: HPO:0000982
Synonyms:
Palmar and plantar keratoderma [HPO:0000982]
Palmoplantar hyperkeratosis [Orphanet:23100]
Palmoplantar Keratosis [Orphanet:23100]
Palmar and plantar keratoderma [OMIM:Palmar and plantar keratoderma]
Palmoplantar keratoderma [OMIM:Palmoplantar keratoderma]
Palmoplantar hyperkeratosis/keratoderma [Orphanet:23100]
Palmoplantar keratoderma [Orphanet:23100]
Palmoplantar keratoderma [MedDRA:10033554]
Keratosis palmaris [MedDRA:10033554]
Tylosis palmaris [MedDRA:10033554]
Hyperkeratosis palmaris and plantaris [MedDRA:10033554]
Keratosis plantaris [MedDRA:10033554]
Keratosis palmaris [OMIM:Keratosis palmaris]
Keratosis plantaris [OMIM:Keratosis plantaris]
Palmoplantar keratoderma (in some patients) [OMIM:Palmoplantar keratoderma (in some patients)]
Quality:
Cross references:
HPO:0007447 "Diffuse palmoplantar hyperkeratosis" [Orphanet:23100]
HPO:0000972 "Palmoplantar hyperkeratosis" [Orphanet:23100]
Orphanet:23100 "Palmoplantar hyperkeratosis/keratoderma" [Orphanet:23100]
OMIM: "Palmar and plantar keratoderma" [OMIM:Palmar and plantar keratoderma]
OMIM: "Palmoplantar keratoderma" [OMIM:Palmoplantar keratoderma]
OMIM: "Keratosis palmaris" [OMIM:Keratosis palmaris]
OMIM: "Keratosis plantaris" [OMIM:Keratosis plantaris]
OMIM: "Palmoplantar keratoderma (in some patients)" [OMIM:Palmoplantar keratoderma (in some patients)]
UMLS:C0022596 "Palmoplantar Keratosis" [Orphanet:23100]
Is a (Direct Parents):
MedDRA Hyperkeratoses
HPO         Hyperkeratosis
Orphanet Abnormality of the skin
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Generalized abnormality of skin(HPO:0011354)
                Abnormality of skin morphology(HPO:0011121)
                   Thickened skin(HPO:0001072)
                      Epidermal thickening(HPO:0011368)
                         Hyperkeratosis(HPO:0000962)
                            Palmoplantar keratoderma(HPO:0000982)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Cornification and dystrophic skin disorders(MedDRA:10011063)
       Hyperkeratoses(MedDRA:10020648)
          Palmoplantar keratoderma(HPO:0000982)
Database Frequency: 40 / 7739
Resource:

All diseases associated with this symptom:

Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Arrhythmogenic right ventricular dysplasia, familial, 11 (OMIM:610476)
Buschke-Ollendorff syndrome (Orphanet:1306)
CEDNIK syndrome (Orphanet:66631)
Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis (OMIM:615821)
Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis (Orphanet:352662)
Diffuse palmoplantar keratoderma with painful fissures (Orphanet:369999)
Ectodermal dysplasia - cutaneous syndactyly syndrome (Orphanet:247827)
Epidermolytic palmoplantar keratoderma (Orphanet:2199)
Exfoliative ichthyosis (Orphanet:289586)
Familial isolated dilated cardiomyopathy (Orphanet:154)
Hereditary palmoplantar keratoderma, Gamborg-Nielsen type (Orphanet:86923)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 10 (OMIM:615024)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A (OMIM:601277)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5 (OMIM:604777)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 (OMIM:612281)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 7 (OMIM:615022)
ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS (OMIM:602540)
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED (OMIM:308800)
KERATOSIS PALMOPLANTARIS STRIATA II (OMIM:612908)
KERATOSIS PALMOPLANTARIS STRIATA III (OMIM:607654)
Keratosis follicularis spinulosa decalvans (Orphanet:2340)
Keratosis palmaris et plantaris - clinodactyly (Orphanet:86919)
Mutilating palmoplantar keratoderma with periorificial keratotic plaques (Orphanet:659)
Naegeli-Franceschetti-Jadassohn syndrome (Orphanet:69087)
Naxos disease (Orphanet:34217)
PACHYONYCHIA CONGENITA 3 (OMIM:615726)
PACHYONYCHIA CONGENITA 4 (OMIM:615728)
PALMOPLANTAR KERATODERMA AND WOOLLY HAIR (OMIM:616099)
PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTICPLAQUES, X-LINKED (OMIM:300918)
PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL (OMIM:613000)
PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL OR DIFFUSE (OMIM:615735)
PEELING SKIN WITH LEUKONYCHIA, ACRAL PUNCTATE KERATOSES, CHEILITIS,AND KNUCKLE PADS (OMIM:616295)
Palmoplantar keratoderma-spastic paralysis syndrome (Orphanet:2201)
Pityriasis rubra pilaris (Orphanet:2897)
Schöpf-Schulz-Passarge syndrome (Orphanet:50944)
Self-healing collodion baby (Orphanet:281122)
Tyrosinemia type 2 (Orphanet:28378)
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome (Orphanet:65282)
[DEL] Arrhythmogenic right ventricular dysplasia, familial, 1 (OMIM:107970)