Achondroplasia
|
(Orphanet:15)
|
Acrocapitofemoral dysplasia
|
(Orphanet:63446)
|
Aortic arch anomaly - peculiar facies - intellectual deficit
|
(Orphanet:1110)
|
BARATELA-SCOTT SYNDROME
|
(OMIM:300881)
|
BLOUNT DISEASE, ADOLESCENT
|
(OMIM:259200)
|
Blount disease
|
(Orphanet:2768)
|
CRANIOMETADIAPHYSEAL DYSPLASIA
|
(OMIM:269300)
|
Carpenter syndrome
|
(Orphanet:65759)
|
DESBUQUOIS DYSPLASIA 1
|
(OMIM:251450)
|
Desbuquois syndrome
|
(Orphanet:1425)
|
Dysplasia epiphysealis hemimelica
|
(Orphanet:1822)
|
Ear-patella-short stature syndrome
|
(Orphanet:2554)
|
FACES syndrome
|
(Orphanet:1969)
|
Gnathodiaphyseal dysplasia
|
(Orphanet:53697)
|
Goldblatt syndrome
|
(Orphanet:166272)
|
Hypocalcemic vitamin D-resistant rickets
|
(Orphanet:93160)
|
Hypochondroplasia
|
(Orphanet:429)
|
Hypophosphatemic rickets, autosomal recessive, 2
|
(OMIM:613312)
|
Ito hypomelanosis
|
(Orphanet:435)
|
Léri-Weill dyschondrosteosis
|
(Orphanet:240)
|
MEIER-GORLIN SYNDROME 3
|
(OMIM:613803)
|
METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS
|
(OMIM:250460)
|
Megalocornea-intellectual deficit syndrome
|
(Orphanet:2479)
|
Mesomelic dwarfism, Nievergelt type
|
(Orphanet:2633)
|
Metaphyseal acroscyphodysplasia
|
(Orphanet:1240)
|
Metaphyseal anadysplasia
|
(Orphanet:1040)
|
Metaphyseal chondrodysplasia, Schmid type
|
(Orphanet:174)
|
Metaphyseal chondrodysplasia, Spahr type
|
(Orphanet:2501)
|
Metaphyseal dysostosis - intellectual deficit - conductive deafness
|
(Orphanet:2502)
|
Microspherophakia - metaphyseal dysplasia
|
(Orphanet:2551)
|
Multiple epiphyseal dysplasia due to collagen 9 anomaly
|
(Orphanet:166002)
|
Multiple epiphyseal dysplasia type 1
|
(Orphanet:93308)
|
Multiple epiphyseal dysplasia type 5
|
(Orphanet:93311)
|
Multiple epiphyseal dysplasia, with miniepiphyses
|
(Orphanet:166032)
|
Multiple non-ossifying fibromatosis
|
(Orphanet:2029)
|
Orofaciodigital syndrome type 4
|
(Orphanet:2753)
|
Pachydermoperiostosis
|
(Orphanet:2796)
|
Pacman dysplasia
|
(Orphanet:1952)
|
Parastremmatic dwarfism
|
(Orphanet:2646)
|
Phocomelia - ectrodactyly - deafness - sinus arrhythmia
|
(Orphanet:2878)
|
Platyspondylic dysplasia, Torrance type
|
(Orphanet:85166)
|
Progressive pseudorheumatoid arthropathy of childhood
|
(Orphanet:1159)
|
Pseudoachondroplasia
|
(Orphanet:750)
|
SMITH-MCCORT DYSPLASIA 1
|
(OMIM:607326)
|
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE
|
(OMIM:609223)
|
SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE
|
(OMIM:611702)
|
Satoyoshi syndrome
|
(Orphanet:3130)
|
Smith-McCort dysplasia
|
(Orphanet:178355)
|
Sotos syndrome
|
(Orphanet:821)
|
Spondylo-megaepiphyseal-metaphyseal dysplasia
|
(Orphanet:228387)
|
Spondyloepimetaphyseal dysplasia - hypotrichosis
|
(Orphanet:168443)
|
Spondyloepimetaphyseal dysplasia congenita, Strudwick type
|
(Orphanet:93346)
|
Spondyloepimetaphyseal dysplasia with multiple dislocations
|
(Orphanet:93360)
|
Spondyloepimetaphyseal dysplasia, Missouri type
|
(Orphanet:93356)
|
Spondyloepimetaphyseal dysplasia, Shohat type
|
(Orphanet:93352)
|
Spondyloepiphyseal dysplasia, Kimberley type
|
(Orphanet:93283)
|
Temtamy syndrome
|
(Orphanet:1777)
|
Thrombocytopenia - absent radius
|
(Orphanet:3320)
|
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR
|
(OMIM:600785)
|
X-linked hypophosphatemia
|
(Orphanet:89936)
|