Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

10 matching diseasesClear search ×

Systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood

Systemic EBV+ T-cell LPD of childhood · Systemic EBV-positive T-cell lymphoproliferative disease of childhood

ORPHA:364033

Chronic lymphoproliferative disorder of natural killer cells

Chronic NK-cell lymphocytosis · Chronic NK lymphocytosis

ORPHA:512017

EBV-induced lymphoproliferative disease due to CARMIL2 deficiency

EBV-induced lymphoproliferative disease due to capping protein regulator and myosin 1 linker 2 deficiency

ORPHA:542301

EBV-induced lymphoproliferative disease due to CD137 deficiency

Epstein-Barr virus-induced lymphoproliferative disease due to Cell differentiation 137 protein deficiency

ORPHA:664726

EBV-induced lymphoproliferative disease due to CD70 deficiency

Epstein-Barr virus-induced lymphoproliferative disease due to CD70 molecule deficiency

ORPHA:538958

EBV-induced lymphoproliferative disease due to PRKCD deficiency

EBV-induced lymphoproliferative disease due to protein kinase C delta deficiency

ORPHA:664711

EBV-induced lymphoproliferative disease due to TET2 deficiency

Epstein-Barr virus-induced lymphoproliferative disease due to tet methylcytosine dioxygenase 2 deficiency

ORPHA:664729

Post-transplant lymphoproliferative disease

PTLD

ORPHA:70568

Primary cutaneous CD30+ T-cell lymphoproliferative disease

Primary cutaneous Ki-1+ T-cell lymphoproliferative disease

ORPHA:541

X-linked lymphoproliferative disease

Duncan disease · Purtilo syndrome

ORPHA:2442