Atelosteogenesis type I
|
(Orphanet:1190)
|
Atelosteogenesis type III
|
(Orphanet:56305)
|
CHST3-related skeletal dysplasia
|
(Orphanet:263463)
|
Caffey disease
|
(Orphanet:1310)
|
Dent disease type 1
|
(Orphanet:93622)
|
FIBULAR APLASIA, TIBIAL CAMPOMELIA, AND OLIGOSYNDACTYLY SYNDROME
|
(OMIM:246570)
|
Geroderma osteodysplastica
|
(Orphanet:2078)
|
Grant syndrome
|
(Orphanet:2097)
|
Growth delay - hydrocephaly - lung hypoplasia
|
(Orphanet:3035)
|
HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE
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(OMIM:300554)
|
Hereditary hypophosphatemic rickets with hypercalciuria
|
(Orphanet:157215)
|
Hypocalcemic vitamin D-dependent rickets
|
(Orphanet:289157)
|
Hypocalcemic vitamin D-resistant rickets
|
(Orphanet:93160)
|
KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS
|
(OMIM:245160)
|
Kyphomelic dysplasia
|
(Orphanet:1801)
|
Léri-Weill dyschondrosteosis
|
(Orphanet:240)
|
Metaphyseal acroscyphodysplasia
|
(Orphanet:1240)
|
Metaphyseal anadysplasia
|
(Orphanet:1040)
|
Microcephalic osteodysplastic primordial dwarfism type 2
|
(Orphanet:2637)
|
Microphthalmia with limb anomalies
|
(Orphanet:1106)
|
OSTEOGENESIS IMPERFECTA, TYPE II
|
(OMIM:166210)
|
OSTEOGENESIS IMPERFECTA, TYPE III
|
(OMIM:259420)
|
OSTEOGENESIS IMPERFECTA, TYPE VIII
|
(OMIM:610915)
|
OSTEOSCLEROSIS WITH ICHTHYOSIS AND FRACTURES
|
(OMIM:166740)
|
Osteodysplasty, Melnick-Needles type
|
(Orphanet:2484)
|
Osteogenesis imperfecta type 2
|
(Orphanet:216804)
|
Osteogenesis imperfecta type 3
|
(Orphanet:216812)
|
Otopalatodigital syndrome
|
(Orphanet:669)
|
Otopalatodigital syndrome type 2
|
(Orphanet:90652)
|
Schinzel-Giedion syndrome
|
(Orphanet:798)
|
Spondyloepimetaphyseal dysplasia, Missouri type
|
(Orphanet:93356)
|
Spondylometaphyseal dysplasia - cone-rod dystrophy
|
(Orphanet:85167)
|
Stüve-Wiedemann syndrome
|
(Orphanet:3206)
|
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B
|
(OMIM:600081)
|
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR
|
(OMIM:600785)
|
X-linked hypophosphatemia
|
(Orphanet:89936)
|