WormMine: DiseaseOntology DOID:0070159 hereditary sensory neuropathy X-linked Disease Ontology

Name
Disease Ontology

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:863	nervous system disease	A disease of anatomical entity that is located_in the central nervous system or located_in the peripheral nervous system.
DOID:574	peripheral nervous system disease	A nervous system disease that affects the peripheral nervous system.
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:870	neuropathy	A nervous system disease that is located_in nerves or nerve cells.
DOID:0050735	X-linked monogenic disease	A monogenic disease that has_material_basis_in mutations in genes on the X chromosome.
DOID:0080012	X-linked recessive disease	A X-linked monogenic disease that has_material_basis_in recessive inheritance.
DOID:0050548	hereditary sensory neuropathy	A neuropathy characterized by congenital insensitivity to pain resulting in ulceration to the fingers, tongue, lips, and other distal appendages.
DOID:0070159	hereditary sensory neuropathy X-linked	A hereditary sensory neuropathy characterized by X-linked inheritance of slowly progressing neuropathy with onset in the first or second decade of life.

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