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"

17 matching diseasesClear search ×

Mesoaxial synostotic syndactyly with phalangeal reduction

MSSD · Syndactyly type 9

ORPHA:157801

Brachydactyly-syndactyly, Zhao type

ORPHA:93409

Cenani-Lenz syndrome

Cenani syndactyly · Cenani-Lenz syndactyly

ORPHA:3258

Syndactyly type 1

ORPHA:93402

Syndactyly type 2

Synpolydactyly

ORPHA:93403

Syndactyly type 3

SD3 · Syndactyly of fingers 4 and 5

ORPHA:93404

Syndactyly type 4

Polysyndactyly, Haas type

ORPHA:93405

Syndactyly type 5

Postaxial syndactyly with metacarpal synostosis · SD5

ORPHA:93406

Syndactyly type 6

Mitten hand · Syndactyly, mitten type

ORPHA:295012

Syndactyly type 8

Fusion of metacarpals 4 and 5

ORPHA:2498

Synpolydactyly type 1

SD2, Vordingborg type · SD2a

ORPHA:295195

Synpolydactyly type 2

SD2, Debeer type · SD2b

ORPHA:295197

Synpolydactyly type 3

SD2, Malik type · SD2c

ORPHA:295199

Zygodactyly type 1

SD1, Weidenreich type · SD1a

ORPHA:295187

Zygodactyly type 2

SD1, Lueken type · SD1b

ORPHA:295189

Zygodactyly type 3

SD1, Montagu type · SD1c

ORPHA:295191

Zygodactyly type 4

SD1, Castilla type · SD1d

ORPHA:295193