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Turner Syndrome (MONDO:0019499)

Open Trait in OLS

Turner syndrome is a chromosomal disorder associated with the complete or partial absence of an X chromosome.

Overview

Category

syndromic disease

reproductive system disorder

endocrine system disorder

Ontology ID

MONDO:0019499

Internal:19317

Synonyms

gonadal dysgenesis

45,X gonadal dysgenesis

45,X syndrome

45,X/46,XX syndrome

45,X0 syndrome

45X syndrome

karyotype 45, X

monosomy X

45, X syndrome

Bonnevie-Ullrich syndrome

Schereshevkii Turner syndrome

Turner Varny syndrome

Ullrich-Turner syndrome

chromosome X monosomy X

genital dwarfism

genital dwarfism, Turner type

gonadal dysgenesis (45,X)

gonadal dysgenesis Turner type

Mapped terms

DOID:3491

GARD:0007831

ICD10CM:Q96.0

ICD10WHO:Q96

ICD9:758.7

MEDGEN:21734

MESH:D014424

MedDRA:10045181

NANDO:2200410

NCIT:C26900

NORD:1806

Orphanet:881

SCTID:38804009

UMLS:C0041408

icd11.foundation:1987089698

Child terms

MONDO:0001969

MONDO:0020466

MONDO:0020472

Results

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