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"

80 matching diseasesClear search ×

Spondylometaphyseal dysplasia, Schmidt type

Spondylometaphyseal dysplasia with severe genu valgum · Spondylometaphyseal dysplasia, Algerian type

ORPHA:93316

Anauxetic dysplasia

Spondyloepimetaphyseal dysplasia, Menger type · Spondyloepimetaphyseal dysplasia, anauxetic type

ORPHA:93347

Autosomal dominant otospondylomegaepiphyseal dysplasia

AD OSMED · Stickler syndrome type 3

ORPHA:166100

Autosomal recessive spondylometaphyseal dysplasia, Mégarbané type

ORPHA:401979

Axial spondylometaphyseal dysplasia

ORPHA:168549

Cartilage-hair hypoplasia

Autosomal recessive metaphyseal chondrodysplasia · Metaphyseal chondrodysplasia, McKusick type

ORPHA:175

Craniometadiaphyseal dysplasia, wormian bone type

ORPHA:85184

Craniometaphyseal dysplasia

ORPHA:1522

EXOC6B-related spondyloepimetaphyseal dysplasia with joint laxity

EXOC6B-SEMD-JL · SEMD-JL3

ORPHA:642085

Frontometaphyseal dysplasia

ORPHA:1826

Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome

Leukoencephalopathy-metaphyseal chondrodysplasia syndrome · H-SMD

ORPHA:83629

Metaphyseal anadysplasia

Maroteaux-Verloes-Stanescu syndrome · Regressive metaphyseal dysplasia

ORPHA:1040

Metaphyseal chondrodysplasia, Jansen type

ORPHA:33067

Metaphyseal chondrodysplasia, Kaitila type

ORPHA:166038

Metaphyseal chondrodysplasia, Rosenberg type

Rosenberg-Lohr syndrome

ORPHA:1837

Metaphyseal chondrodysplasia, Schmid type

MDSC · SMCD

ORPHA:174

Metaphyseal chondrodysplasia, Spahr type

ORPHA:2501

Metaphyseal dysplasia, Braun-Tinschert type

ORPHA:85188

MGP-related spondyloepiphyseal dysplasia

MGP-related SED · Spondyloepiphyseal dysplasia-platyspondyly-brachytelephalangism syndrome

ORPHA:664377

MIR140-related spondyloepiphyseal dysplasia

MIR140-related SED · Spondyloepiphyseal dysplasia with severe brachydactyly-cone-shaped epiphyses

ORPHA:623695

Multiple epiphyseal dysplasia type 1

EDM1 · MED1

ORPHA:93308

Multiple epiphyseal dysplasia type 4

Autosomal recessive multiple epiphyseal dysplasia · EDM4

ORPHA:93307

Multiple epiphyseal dysplasia type 5

Bilateral hereditary micro-epiphyseal dysplasia · BHMED

ORPHA:93311

Multiple epiphyseal dysplasia type 7

MED7 · EDM7

ORPHA:647676

Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome

Multiple epiphyseal dysplasia, Al-Gazali type

ORPHA:166024

Multiple metaphyseal dysplasia

ORPHA:93430

OBSOLETE: Spondyloepimetaphyseal dysplasia

ORPHA:252

OBSOLETE: Spondyloepimetaphyseal dysplasia with joint laxity

ORPHA:93359

OBSOLETE: Spondyloepimetaphyseal dysplasia with severe short stature

ORPHA:642737

OBSOLETE: Unclassified spondylometaphyseal dysplasia

ORPHA:163678

Pseudoachondroplasia

Pseudoachondroplastic dysplasia · Pseudoachondroplastic spondyloepiphyseal dysplasia

ORPHA:750

Pyle disease

SFRP4-related Pyle disease · Metaphyseal dysplasia, Pyle type

ORPHA:3005

Regressive spondylometaphyseal dysplasia

ORPHA:448267

SBDS-related severe neonatal spondylometaphyseal dysplasia

Spondylometaphyseal dysplasia, Sedaghatian-like type · SBDS-related severe neonatal SMD

ORPHA:622934

Schimke immuno-osseous dysplasia

Schimke syndrome · Spondyloepiphyseal dysplasia-nephrotic syndrome

ORPHA:1830

SPONASTRIME dysplasia

Spondylar and nasal changes with striations of the metaphyses (SPONASTRIME) dysplasia · Spondyloepimetaphyseal dysplasia, Sponastrime type

ORPHA:93357

Spondylo-megaepiphyseal-metaphyseal dysplasia

ORPHA:228387

Spondylodysplastic dysplasia

ORPHA:93434

Spondyloenchondrodysplasia

SPENCD · Spondyloenchondromatosis

ORPHA:1855

Spondyloepimetaphyseal dysplasia congenita, Strudwick type

ORPHA:93346

Spondyloepimetaphyseal dysplasia with joint laxity, Beighton type

SEMD-JL1 · Spondyloepimetaphyseal dysplasia with joint laxity type 1

ORPHA:642099

Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type

SEMD-MD · SEMDJL2

ORPHA:93360

Spondyloepimetaphyseal dysplasia-abnormal dentition syndrome

SEMDAD

ORPHA:168451

Spondyloepimetaphyseal dysplasia-hypotrichosis syndrome

ORPHA:168443

Spondyloepimetaphyseal dysplasia, aggrecan type

SEMD, aggrecan type

ORPHA:171866

Spondyloepimetaphyseal dysplasia, Bieganski type

ORPHA:168448

Spondyloepimetaphyseal dysplasia, Geneviève type

SEMD, Geneviève type · SEMDG

ORPHA:168454

Spondyloepimetaphyseal dysplasia, Handigodu type

ORPHA:99642