WormMine

WS295

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0111709 focal nonepidermolytic palmoplantar keratoderma 1 Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  A focal nonepidermolytic palmoplantar keratoderma that has_material_basis_in heterozygous mutation in the KRT16 gene on chromosome 17q21.2.

1 Ontology

Name
Disease Ontology

13 Parents

Identifier Name Description
DOID:7 disease of anatomical entity A disease that manifests in a defined anatomical structure.
DOID:4 disease A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism.
DOID:37 skin disease An integumentary system disease that is located_in skin.
DOID:16 integumentary system disease A disease of anatomical entity that is located_in the integumentary system comprising the skin and its appendages.
DOID:0050177 monogenic disease A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive.
DOID:630 genetic disease A disease that has_material_basis_in genetic variations in the human genome.
DOID:0050736 autosomal dominant disease An autosomal genetic disease that is characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease.
DOID:0050739 autosomal genetic disease A monogenic disease that has_material_basis_in a mutation in a single gene on one of the non-sex chromosomes.
DOID:3390 palmoplantar keratosis A keratosis characterized by abnormal thickening of the palms and the soles.
DOID:0050428 nonepidermolytic palmoplantar keratoderma A palmoplantar keratosis characterized by a well-demarcated, symmetric keratoderma located_in palms and located_in soles.
DOID:161 keratosis A skin disease characterized_by growth of keratin on the skin or mucous membranes.
DOID:0111708 focal nonepidermolytic palmoplantar keratoderma A nonepidermolytic palmoplantar keratoderma characterized by localized areas of hyperkeratosis located mainly on pressure points and sites of recurrent friction.
DOID:0111709 focal nonepidermolytic palmoplantar keratoderma 1 A focal nonepidermolytic palmoplantar keratoderma that has_material_basis_in heterozygous mutation in the KRT16 gene on chromosome 17q21.2.

12 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:0111708 DOID:0111709
is_a DOID:0050736 DOID:0111709
is_a DOID:3390 DOID:0111709
is_a DOID:630 DOID:0111709
is_a DOID:0050739 DOID:0111709
is_a DOID:0050177 DOID:0111709
is_a DOID:37 DOID:0111709
is_a DOID:0050428 DOID:0111709
is_a DOID:161 DOID:0111709
is_a DOID:7 DOID:0111709
is_a DOID:4 DOID:0111709
is_a DOID:16 DOID:0111709

1 Synonyms

Name Type
FNEPPK1 synonym