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"

40 matching diseasesClear search ×

Familial calcium pyrophosphate deposition

Calcium pyrophosphate dihydrate crystal deposition disease · Familial CC

ORPHA:1416

Autosomal systemic lupus erythematosus

Autosomal SLE · Disseminated lupus erythematosus

ORPHA:300345

Benign hereditary chorea

BHC · Benign familial chorea

ORPHA:1429

Congenital thrombotic thrombocytopenic purpura

Congenital ADAMTS-13 deficiency · Congenital TTP

ORPHA:93583

Familial adenomatous polyposis

Colorectal adenomatous polyposis · FAP

ORPHA:733

Familial anetoderma

Hereditary anetoderma · Hereditary macular atrophy

ORPHA:228277

Familial articular hypermobility syndrome

Familial joint instability syndrome · Familial joint laxity

ORPHA:2295

Familial atrial myxoma

ORPHA:615

Familial bicuspid aortic valve

Familial BAV

ORPHA:402075

Familial caudal dysgenesis

Rudd-Klimek syndrome

ORPHA:1768

Familial cavitary optic disc anomaly

Familial CODA

ORPHA:464760

Familial cerebral cavernous malformation

Familial brain cavernous angioma · Familial cerebral cavernoma

ORPHA:221061

Familial Chilblain lupus

ORPHA:481662

Familial cold urticaria

FCAS · FCU

ORPHA:47045

Familial cylindromatosis

Turban tumor syndrome

ORPHA:211

Familial drusen

DHRD · Dominant drusen

ORPHA:75376

Familial dysautonomia

HSAN3 · Hereditary sensory and autonomic neuropathy type 3

ORPHA:1764

Familial hemophagocytic lymphohistiocytosis

Familial HLH · Hemophagocytic lymphohistiocytosis

ORPHA:540

Familial infantile bilateral striatal necrosis

Familial IBSN · Familial infantile striatonigral degeneration

ORPHA:225154

Familial isolated café-au-lait macules

Familial isolated CALSs · Multiple isolated café-au-lait spots

ORPHA:2678

Familial melanoma

ORPHA:618

Familial multinodular goiter

Familial multinodular goiter syndrome · FMNG

ORPHA:276399

Familial nasal acilia

ORPHA:922

Familial pancreatic carcinoma

Familial pancreatic cancer

ORPHA:1333

Familial porencephaly

ORPHA:99810

Familial prostate cancer

ORPHA:1331

Familial sinus histiocytosis with massive lymphadenopathy

Familial Rosaï-Dorfman disease · Familial SHML

ORPHA:254712

Familial syringomyelia

ORPHA:370034

Familial thoracic aortic aneurysm and aortic dissection

Familial TAAD · FTAAD

ORPHA:91387

Familial vesicoureteral reflux

Familial VUR

ORPHA:289365

Fatal familial insomnia

FFI

ORPHA:466

Hereditary breast cancer

Familial breast cancer · Familial breast carcinoma

ORPHA:227535

Hyperkalemic periodic paralysis

Adynamia episodica hereditaria · Familial hyperPP

ORPHA:682

Inherited acute myeloid leukemia

Acute myeloid leukemia · AML

ORPHA:319465

Isolated familial medullary thyroid carcinoma

Hereditary isolated MTC · Isolated familial MTC

ORPHA:99361

Juvenile Paget disease

Familial osteoectasia · Hereditary hyperphosphatasia

ORPHA:2801

OBSOLETE: Familial cervical artery dissection

OBSOLETE: Familial CAD · OBSOLETE: Hereditary CAD

ORPHA:36382

Paroxysmal extreme pain disorder

Familial rectal pain

ORPHA:46348

Paroxysmal kinesigenic dyskinesia

Familial PKD · Familial paroxysmal kinesigenic dyskinesia

ORPHA:98809

Susceptibility to respiratory infections associated with CD8alpha chain mutation

Familial CD8 deficiency

ORPHA:169085