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"

11 matching diseasesClear search ×

Primary cutaneous amyloidosis

PLCA · Primary localized cutaneous amyloidosis

ORPHA:137807

Familial primary localized cutaneous amyloidosis

FPLCA

ORPHA:353220

Nodular cutaneous amyloidosis

PLCNA · Primary localized cutaneous nodular amyloidosis

ORPHA:137810

Primary cutaneous B-cell lymphoma

ORPHA:178563

Primary cutaneous lymphoma

ORPHA:542

Primary cutaneous plasmacytosis

ORPHA:451602

Primary cutaneous T-cell lymphoma

CTCL · Mycosis fungoides

ORPHA:171901

Primary cutaneous tuberculosis

Primary skin tuberculosis

ORPHA:645849

Primary localized amyloidosis

Localized AL amyloidosis

ORPHA:314709

Primary systemic amyloidosis

Systemic AL amyloidosis

ORPHA:314701

X-linked reticulate pigmentary disorder

Familial cutaneous amyloidosis · PDR

ORPHA:85453