| Disease Browser
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Parent Node:
 Foot Deformities, Congenital (D005532) | Parent Node:
Hair Diseases (D006201) | Parent Node:
Hand Deformities, Congenital (D006228) | Parent Node:
Skin Abnormalities (D012868) | ..Starting node
.. Hairy palms and soles (C535620)
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Child Nodes:
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Sister Nodes: | ..Acrodermatitis (D000169)  1
| ..Anetoderma (D057088) 2
| ..Arthropathy, Erosive (C565273)
| ..Barber Say syndrome (C537908)
| ..Blepharophimosis syndrome type 1 (C536233)
| ..Blepharophimosis syndrome type 2 (C536234)
| ..Blepharophimosis with ptosis, syndactyly, and short stature (C536235)
| ..Blepharophimosis, Ptosis, and Epicanthus Inversus (C562419)
| ..Book Syndrome (C562993)
| ..Carney Complex (D056733) 1
| ..COCOON SYNDROME (OMIM:613630)
| ..Comedones, Familial Dyskeratotic (C562838)
| ..Cutis Gyrata Syndrome of Beare And Stevenson (C565129)
| ..Dermal Ridges, Nelson Syndrome (C565110)
| ..Dermal Ridges, Patternless (C565109)
| ..Dermoodontodysplasia (C565103)
| ..Dyskeratosis Congenita (D019871) 3
| ..Dyskeratosis, Hereditary Benign Intraepithelial (C562551)
| ..Ectodermal Dysplasia (D004476) 144
| ..Ehlers-Danlos Syndrome (D004535) 23
| ..Epidermolysis Bullosa (D004820) 29
| ..Epithelial Squamous Dysplasia, Keratinizing Desquamative, of Urinary Tract (C565584)
| ..Familial popliteal pterygium syndrome (C535891)
| ..Hairy palms and soles (C535620)
| ..Hemangiomatosis, Cutaneous, with Associated Features (C562438)
| ..Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated With Cerebral Capillary Malformations (C566153)
| ..Hypohidrosis aith Abnormal Palmar Dermal Ridges (C565481)
| ..Ichthyosis (D007057) 66
| ..Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin (C563402)
| ..Incontinentia Pigmenti (D007184) 2
| ..Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma (C566600)
| ..Michelin tire baby syndrome (C537575)
| ..Microphthalmia, syndromic 7 (C537466)
| ..Multiple pterygium syndrome (C537377) 1
| ..Oculocerebrocutaneous syndrome (C538088)
| ..Poikiloderma with Neutropenia (C565820)
| ..Poikiloderma, Hereditary Sclerosing (C562824)
| ..Port-Wine Stain (D019339) 4
| ..Prolidase Deficiency (D056732)
| ..Pseudoxanthoma Elasticum (D011561) 2
| ..Pterygium Colli, Isolated (C566741)
| ..Ridges-off-the-end syndrome (C531754)
| ..Rothmund-Thomson Syndrome (D011038) 5
| ..Sclerema Neonatorum (D012593)
| ..Skin/Hair/Eye Pigmentation, Variation In, 10 (C567376)
| ..Skin/Hair/Eye Pigmentation, Variation In, 11 (C567374)
| ..Skin/Hair/Eye Pigmentation, Variation In, 4 (C567300)
| ..Skin/Hair/Eye Pigmentation, Variation In, 5 (C567119)
| ..Skin/Hair/Eye Pigmentation, Variation In, 6 (C567139)
| ..Skin/Hair/Eye Pigmentation, Variation In, 7 (C567155)
| ..Skin/Hair/Eye Pigmentation, Variation In, 8 (C567096)
| ..Skin/Hair/Eye Pigmentation, Variation In, 9 (C567091)
| ..Tight skin contracture syndrome, lethal (C536920)
| ..Trichothiodystrophy Syndromes (D054463) 5
| ..Urban Schosser Spohn syndrome (C536476)
| ..Vascular Hyalinosis (C564750)
| ..Winter Shortland Temple syndrome (C536735)
| ..Xeroderma Pigmentosum (D014983) 16
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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| Term ID: | 4863 |
| Name: | Hairy palms and soles |
| Definition: | |
| Alternative IDs: | |
| ParentIDs: | MESH:D005532|MESH:D006201|MESH:D006228|MESH:D012868 |
| TreeNumbers: | C05.330.495/C535620 |C05.390.408/C535620 |C05.660.585.512.380/C535620 |C05.660.585.988.425/C535620 |C16.131.621.585.380/C535620 |C16.131.621.585.425/C535620 |C16.131.831/C535620 |C17.800.329/C535620 |C17.800.804/C535620 |
| Synonyms: | Circumscribed hairy dysembryoplasia of palms |Hairy cutaneous malformations of palms and soles |Thickened hair-bearing skin on the palms of both hands |
| Slim Mappings: | Congenital abnormality|Musculoskeletal disease|Skin disease |
| Reference: |
MedGen: C535620
MeSH: C535620
OMIM: 139650;
Genes: | | Phenotypes | | | Disease Causing ClinVar Variants | |
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