WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0050541 Charcot-Marie-Tooth disease type 4 Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  A Charcot-Marie-Tooth disease characterized by demyelinating or axonal abnormalities that has_material_basis_in autosomal recessive inheritance.

1 Ontology

Name
Disease Ontology

9 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: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:17 musculoskeletal system disease A disease of anatomical entity that occurs in the muscular and/or skeletal system.
DOID:870 neuropathy A nervous system disease that is located_in nerves or nerve cells.
DOID:440 neuromuscular disease A neuropathy that affect the nerves that control the voluntary muscles.
DOID:10595 Charcot-Marie-Tooth disease A neuromuscular disease that is characterized by a slowly progressive degeneration of the muscles of the foot, lower leg, hand and forearm.
DOID:0050541 Charcot-Marie-Tooth disease type 4 A Charcot-Marie-Tooth disease characterized by demyelinating or axonal abnormalities that has_material_basis_in autosomal recessive inheritance.

21 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:10595 DOID:0050541
is_a DOID:17 DOID:0050541
is_a DOID:440 DOID:0050541
is_a DOID:574 DOID:0050541
is_a DOID:870 DOID:0050541
is_a DOID:4 DOID:0050541
is_a DOID:7 DOID:0050541
is_a DOID:863 DOID:0050541
is_a DOID:0050541 DOID:0051028
is_a DOID:0050541 DOID:0110183
is_a DOID:0050541 DOID:0110184
is_a DOID:0050541 DOID:0110185
is_a DOID:0050541 DOID:0110186
is_a DOID:0050541 DOID:0110187
is_a DOID:0050541 DOID:0110190
is_a DOID:0050541 DOID:0110191
is_a DOID:0050541 DOID:0110192
is_a DOID:0050541 DOID:0110193
is_a DOID:0050541 DOID:0110194
is_a DOID:0050541 DOID:0110195
is_a DOID:0050541 DOID:0110196

2 Synonyms

Name Type
hereditary motor and sensory neuropathy synonym
DOID:0050582 alt_id