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■ Abbreviation / Long Form : FPH / Familial progressive hyperpigmentation

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Total Number of Papers: 7
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Abbreviation:   FPH  (>> Co-occurring Abbreviation)
Long Form:   Familial progressive hyperpigmentation
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No. Year Title Co-occurring Abbreviation
2017 Familial Progressive Hyperpigmentation, Cutaneous Mastocytosis, and Gastrointestinal Stromal Tumor as Clinical Manifestations of Mutations in the c-KIT Receptor Gene. ---
2017 Familial progressive hyperpigmentation: A family resurvey and ultrastructural skin investigation. ---
2012 Familial progressive hyperpigmentation: a case report. ---
2011 KITLG mutations cause familial progressive hyper- and hypopigmentation. DUH2, FPHH
2009 A kindred with familial progressive hyperpigmentation-like disorder: implication of fibroblast-derived growth factors in pigmentation. HGF, KGF, SCF
2009 Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation. KITLG
2006 Linkage of a locus determining familial progressive hyperpigmentation (FPH) to chromosome 19p13.1-pter in a Chinese family. PJS