WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0070554 palmoplantar keratoderma and woolly hair Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  A nonepidermolytic palmoplantar keratoderma characterized by striate palmoplantar keratoderma, sparse and woolly hair, leukonychia, and the absence of cardiomyopathy symptoms or findings on echocardiography and electrocardiogram that has_material_basis_in homozygous mutation in the KANK2 gene on chromosome 19p13.2.

1 Ontology

Name
Disease Ontology

12 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: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:0050737 autosomal recessive disease An autosomal genetic disease that is characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop.
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:0070554 palmoplantar keratoderma and woolly hair A nonepidermolytic palmoplantar keratoderma characterized by striate palmoplantar keratoderma, sparse and woolly hair, leukonychia, and the absence of cardiomyopathy symptoms or findings on echocardiography and electrocardiogram that has_material_basis_in homozygous mutation in the KANK2 gene on chromosome 19p13.2.

11 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:0050737 DOID:0070554
is_a DOID:0050428 DOID:0070554
is_a DOID:630 DOID:0070554
is_a DOID:0050177 DOID:0070554
is_a DOID:4 DOID:0070554
is_a DOID:37 DOID:0070554
is_a DOID:3390 DOID:0070554
is_a DOID:161 DOID:0070554
is_a DOID:16 DOID:0070554
is_a DOID:0050739 DOID:0070554
is_a DOID:7 DOID:0070554

3 Synonyms

Name Type
keratoderma with woolly hair type IV synonym
PPKWH synonym
woolly hair-palmoplantar keratoderma syndrome type 4 synonym