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Ehlers-Danlos syndrome, autosomal dominant, type unspecified

MedGen UID:
65083
Concept ID:
C0220679
Disease or Syndrome
Synonyms: EDS, UNSPECIFIED TYPE; EHLERS-DANLOS SYNDROME, FRIEDMAN-HARROD TYPE
 
Monarch Initiative: MONDO:0007528
OMIM®: 130090

Recent clinical studies

Etiology

Esaka EJ, Golde SH, Stever MR, Thomas RL
Obstet Gynecol 2009 Feb;113(2 Pt 2):515-518. doi: 10.1097/AOG.0b013e3181898cbf. PMID: 19155940

Diagnosis

Esaka EJ, Golde SH, Stever MR, Thomas RL
Obstet Gynecol 2009 Feb;113(2 Pt 2):515-518. doi: 10.1097/AOG.0b013e3181898cbf. PMID: 19155940

Prognosis

Esaka EJ, Golde SH, Stever MR, Thomas RL
Obstet Gynecol 2009 Feb;113(2 Pt 2):515-518. doi: 10.1097/AOG.0b013e3181898cbf. PMID: 19155940

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