disease arises from structure disease arises from alteration in structure chromosome X (Human) gonadal dysgenesis syndromic disease sex chromosome disorder of sex development Turner syndrome https://github.com/monarch-initiative/mondo/issues/6744 https://github.com/monarch-initiative/mondo/issues/9097 https://rarediseases.info.nih.gov/diseases/2458/genital-dwarfism https://rarediseases.info.nih.gov/diseases/2540/gonadal-dysgenesis-turner-type https://rarediseases.info.nih.gov/diseases/7831/turner-syndrome https://www.malacards.org/card/turner_syndrome 45X syndrome 45,X0 syndrome Orphanet:881 Schereshevkii Turner syndrome NORD:1806 gonadal dysgenesis SCTID:38804009 ICD9:758.7 monosomy X genital dwarfism 45,X/46,XX syndrome MESH:D014424 NANDO:2200410 gonadal dysgenesis Turner type 45,X gonadal dysgenesis genital dwarfism, Turner type Turner Varny syndrome MEDGEN:21734 45,X syndrome gonadal dysgenesis (45,X) ICD10WHO:Q96 icd11.foundation:1987089698 45, X syndrome UMLS:C0041408 karyotype 45, X ICD10CM:Q96.0 chromosome X monosomy X GARD:0007831 DOID:3491 MONDO:0019499 MedDRA:10045181 Turner syndrome is a chromosomal disorder associated with the complete or partial absence of an X chromosome. Ullrich-Turner syndrome NCIT:C26900 inherited primary ovarian failure obsolete chromosomal anomaly with cataract