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"

200 matching diseasesClear search ×

Bartter syndrome type 1

Bartter syndrome type I

ORPHA:620217

Bartter syndrome type 2

Bartter syndrome type II

ORPHA:620220

Bartter syndrome type 3

Bartter syndrome type III

ORPHA:93605

Bartter syndrome type 4

Bartter syndrome with sensorineural hearing loss · Bartter syndrome with sensorineural deafness

ORPHA:89938

46,XY complete gonadal dysgenesis

46,XY CGD · 46,XY pure gonadal dysgenesis

ORPHA:242

Aase-Smith syndrome type 1

Aase-Smith I syndrome · Hydrocephalus-cleft palate-joint contractures syndrome

ORPHA:916

Absence of fingerprints-congenital milia syndrome

Absence of dermatoglyphics-congenital milia syndrome · Baird syndrome

ORPHA:1658

Acquired partial lipodystrophy

Barraquer-Simons syndrome · Progressive cephalothoracic lipodystrophy

ORPHA:79087

ALG1-CDG

CDG syndrome type Ik · CDG-Ik

ORPHA:79327

ALG11-CDG

CDG syndrome type Ip · CDG-Ip

ORPHA:280071

ALG12-CDG

CDG syndrome type Ig · CDG-Ig

ORPHA:79324

ALG13-CDG

Congenital disorder of glycosylation type Is · CDG syndrome type Is

ORPHA:324422

ALG2-CDG

CDG syndrome type Ii · CDG-Ii

ORPHA:79326

ALG3-CDG

CDG syndrome type Id · CDG-Id

ORPHA:79321

ALG6-CDG

CDG syndrome type Ic · CDG-Ic

ORPHA:79320

ALG8-CDG

CDG syndrome type Ih · CDG-Ih

ORPHA:79325

ALG9-CDG

CDG syndrome type IL · CDG1L

ORPHA:79328

Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16

ATR syndrome linked to chromosome 16 · ATR syndrome, deletion type

ORPHA:98791

Andersen-Tawil syndrome

Andersen syndrome · LQT7

ORPHA:37553

Arthrochalasia Ehlers-Danlos syndrome

EDS VII · Ehlers-Danlos syndrome type 7

ORPHA:1899

Ataxia-telangiectasia

Louis-Bar syndrome

ORPHA:100

Autosomal dominant otospondylomegaepiphyseal dysplasia

AD OSMED · Stickler syndrome type 3

ORPHA:166100

Autosomal recessive spastic paraplegia type 20

Childhood-onset spastic paraparesis-distal muscle wasting syndrome · SPG20

ORPHA:101000

B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome

BILU syndrome · Hoffman syndrome

ORPHA:567502

B4GALT1-CDG

Beta-1,4-galactosyltransferase deficiency · CDG syndrome type IId

ORPHA:79332

Balint syndrome

Balint-Holmes syndrome · Optic ataxia-gaze apraxia-simultanagnosia syndrome

ORPHA:363746

Ballard syndrome

Pitt-Williams brachydactyly · Brachydactyly, combined B and E types

ORPHA:93395

Bamforth-Lazarus syndrome

Athyroidal hypothyroidism-spiky hair-cleft palate syndrome · Bamforth syndrome

ORPHA:1226

Bangstad syndrome

Ataxia-diabetes-goiter-gonadal insufficiency syndrome

ORPHA:1227

Banki syndrome

ORPHA:1228

Barber-Say syndrome

Hypertrichosis-atrophic skin-ectropion-macrostomia syndrome

ORPHA:1231

Bardet-Biedl syndrome

BBS

ORPHA:110

Barth syndrome

3-methylglutaconic aciduria type 2 · BTHS

ORPHA:111

Bartsocas-Papas syndrome

Autosomal recessive popliteal pterygium syndrome · Lethal popliteal pterygium syndrome

ORPHA:1234

Bartter syndrome

Renal tubular normotensive hypokalemic alkalosis with hypercalciuria · Salt-losing tubular disorder, Henle's loop type

ORPHA:112

Bartter syndrome with hypocalcemia

ORPHA:263417

Bazex syndrome

Acrokeratosis of Bazex · Acrokeratosis paraneoplastica

ORPHA:166113

Behr syndrome

Behr complicated familial optic atrophy

ORPHA:1239

BIDS syndrome

Amish brittle hair syndrome · Trichothiodystrophy type D

ORPHA:1245

Biemond syndrome type 2

Hypogonadism-short stature-coloboma-preaxial polydactyly syndrome

ORPHA:141333

Biliary atresia with splenic malformation syndrome

BASM syndrome

ORPHA:244283

Birk-Barel syndrome

Intellectual disability-hypotonia-facial dysmorphism syndrome · Birk-Barel Intellectual Disability-Dimorphism syndrome

ORPHA:166108

Blau syndrome

ORPHA:90340

Blepharo-cheilo-odontic syndrome

BCD syndrome · Blepharocheilodontic syndrome

ORPHA:1997

Blue rubber bleb nevus

Bean syndrome · BRBN

ORPHA:1059

BNAR syndrome

Bifid nose with or without anorectal and renal anomalies

ORPHA:217266

Bohring-Opitz syndrome

BOS syndrome · Bohring syndrome

ORPHA:97297

Böök syndrome

ORPHA:1262