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Total number of diseases with letter "P" in database: 573

A -B -C -D -E -F -G -H -I -J -K -L -M -N -O -P -Q -R -S -T -U -V -W -X -Y - Z

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Records: 136 - 150

136: Peptidase D (PEPD)
137: Perilymphatic gusher during stapes surgery
138: Perilymphatic Gusher-deafness syndrome
139: Periodic fever, Dutch type
140: Periodic fever, familial, autosomal dominant
141: Periodic fever, familial, autosomal dominant
142: Peripheral Myelin Protein 22 (PMP22)
143: Peripherin 2, mouse, homolog of
144: Peripherin, photoreceptor type
145: Peripherin; PRPH
146: Peroneal muscular atrophy
147: Peroxisomal alanine:glyoxylate aminotransferase deficiency
148: Persistent hyperinsulinemic hypoglycemia of infancy (PHHI)
149: Persistent hyperinsulinemic hypoglycemia of infancy due to total adenomatous hyperplasia
150: PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY; PHHI // NESIDIOBLASTOSIS

Should you not find the disease for which you are searching, please send an email to EDDNAL: eddnal@skypro.be

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