Online Directory

Section 1A

Disorders MIM Genes MIM Specialties Commissioning
Ullrich Congenital Muscular Dystrophy; UCMD1 254090
collagen, type VI, alpha 1; COL6A1 120220
collagen, type VI, alpha 2; COL6A2 120240
collagen, type VI, alpha 3 chain; COL6A3 120250
  • Neurology, Paediatric
  • Highly Specialised Services
Uniparental Disomy, Chromosome 16 0
uniparental disomy chromosome 16 0
  • Clinical Genetics
Kagami-Ogata Syndrome 608149
uniparental disomy, paternal, chromosome 14; UPD14 608149
  • Clinical Genetics

Section 1B

Disorders MIM Genes MIM Specialties Commissioning
Uterine Cancer, Familial, 9 Gene Panel 0
...see test listing on database for full details 0
  • Clinical Genetics

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