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DO Term : Turner syndrome [DOID:3491] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A gonadal dysgenesis that is characterized by short stature and early loss of ovarian function resulting from ovarian hypofunction or premature ovarian failure and has_material_basis_in one missing or structurally altered X chromosome.

synonyms:
ICD10CM:Q96,
MESH:D014424,
GARD:7831,
XO syndrome,
Gonadal dysgenesis - Turner,
UMLS_CUI:C1527168,
Karyotype 45, X,
GARD:2540,
SNOMEDCT_US_2023_03_01:38804009,
monosomy X syndrome,
NCI:C34434,
NCI:C26900,
DOID:5448,
Bonnevie-Ullrich syndrome,
Monosomy X,
UMLS_CUI:C0041408

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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