Disease_May_Have_Associated_Disease
Pediatric Endocrinology Terminology
Cellosaurus Disease Terminology
ACC/AHA Pediatric and Congenital Cardiology EHR Terminology
GCT Authorized Value Terminology
GCT Medical History Table
Personal Medical History
Cellosaurus Terminology
Turner Syndrome
45,X Gonadal Dysgenesis
45,X0 Syndrome
45X Syndrome
A chromosomal abnormality occurring in phenotypic females, characterized by the absence of a part or all of one of the sex chromosomes.
A condition caused by absence of part or all of the second sex chromosome in an individual with female phenotype, resulting in a variable constellation of physical and functional anomalies. Characteristic clinical features may include, but are not limited to, short stature, premature ovarian failure, cardiac anomalies, renal anomalies, skeletal variations, and hearing impairment.
A gonadal dysgenesis syndrome occurring in phenotypic females, characterized by the absence of a part or all of one of the sex chromosomes. Signs and symptoms include short stature, webbing of neck, low-set ears, hypogonadism, and sterility.
ACC/AHA
Bonnevie-Ullrich Syndrome
C0041408
C26900
Cellosaurus
Disease or Syndrome
Gonadal Dysgenesis
Monosomy X
NICHD
PCDC
Turner Syndrome
Turner Syndrome
Turner syndrome
Turner_s_Syndrome
Ullrich-Turner Syndrome
Endocrine Syndrome
Non-Neoplastic Endocrine Disorder
Cystic Hygroma
Rare Non-Neoplastic Disorder
Gonadal Dysgenesis
Atypical Polypoid Adenomyoma
NICHD Terminology
Neonatal Research Network Terminology