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Results: 1 to 20 of 33

Make selection to find tests for any of the checked conditions.[x]
ConditionsSynonyms
Fanconi anemia complementation group F
Methylmalonic aciduria and homocystinuria type cblF
  • COBALAMIN F DISEASE
  • COBALAMIN, DEFECT IN LYSOSOMAL RELEASE OF
  • METHYLMALONIC ACIDEMIA AND HOMOCYSTINURIA, cblF TYPE
  • METHYLMALONIC ACIDURIA DUE TO VITAMIN B12-RELEASE DEFECT
  • VITAMIN B12 LYSOSOMAL RELEASE DEFECT
  • VITAMIN B12 STORAGE DISEASE
Xeroderma pigmentosum, group F
  • ERCC4-Related Xeroderma Pigmentosum
  • XERODERMA PIGMENTOSUM VI
  • XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F
  • XERODERMA PIGMENTOSUM, TYPE F
  • XP, GROUP F
  • Xeroderma pigmentosum, type 6
Bosch-Boonstra-Schaaf optic atrophy syndrome
Peroxisome biogenesis disorder 5B
Peroxisome biogenesis disorder 5A (Zellweger)
Charcot-Marie-Tooth disease dominant intermediate F
Glaucoma 1, open angle, F
VACTERL with hydrocephalus
  • VACTERL association with hydrocephalus
  • VACTERL-H
Fetal hemoglobin quantitative trait locus 1
Van den Ende-Gupta syndrome
  • Blepharophimosis, arachnodactyly, and congenital contractures
  • Marden Walker like syndrome
  • Marden Walker like syndrome without psychomotor retardation
Breasts and/or nipples, aplasia or hypoplasia of, 2
Acropectorovertebral dysplasia
  • Acropectorovertebral dysplasia F form
  • F syndrome
Fetal hemoglobin quantitative trait locus 2
Lissencephaly with cerebellar hypoplasia type F
Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
Peroxisome biogenesis disorder, complementation group 10
  • PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP F
Lissencephaly with cerebellar hypoplasia
Niemann-Pick disease, type B
beta Thalassemia
  • Cooley's anemia
  • Erythroblastic anemia
  • Mediterranean anemia

Results: 1 to 20 of 33

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