WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0112183 familial thyroid dyshormonogenesis Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  A congenital hypothyroidism characterized by thyroid hormone deficiency that is present from birth and results from defects in thyroid hormone synthesis.

1 Ontology

Name
Disease Ontology

8 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:28 endocrine system disease A disease of anatomical entity that is located_in endocrine glands which secretes a type of hormone directly into the bloodstream to regulate the body.
DOID:1459 hypothyroidism A thyroid gland disease which involves an underproduction of thyroid hormone.
DOID:0050328 congenital hypothyroidism A hypothyroidism that is present at birth.
DOID:0080015 physical disorder A disease that has_material_basis_in a genetic abnormality, error with embryonic development, infection or compromised intrauterine environment.
DOID:50 thyroid gland disease An endocrine system disease that is located_in the thyroid.
DOID:0112183 familial thyroid dyshormonogenesis A congenital hypothyroidism characterized by thyroid hormone deficiency that is present from birth and results from defects in thyroid hormone synthesis.

13 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:0050328 DOID:0112183
is_a DOID:4 DOID:0112183
is_a DOID:1459 DOID:0112183
is_a DOID:0080015 DOID:0112183
is_a DOID:50 DOID:0112183
is_a DOID:28 DOID:0112183
is_a DOID:7 DOID:0112183
is_a DOID:0112183 DOID:0112184
is_a DOID:0112183 DOID:0112185
is_a DOID:0112183 DOID:0112186
is_a DOID:0112183 DOID:0112187
is_a DOID:0112183 DOID:0112188
is_a DOID:0112183 DOID:0112189

0 Synonyms