Childhood-onset hypophosphatasia
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(Orphanet:247667)
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Craniometadiaphyseal dysplasia, wormian bone type
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(Orphanet:85184)
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Cutis marmorata telangiectatica congenita
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(Orphanet:1556)
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Dent disease type 1
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(Orphanet:93622)
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Diaphyseal medullary stenosis - bone malignancy
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(Orphanet:85182)
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FANCONI RENOTUBULAR SYNDROME 3
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(OMIM:615605)
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Gnathodiaphyseal dysplasia
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(Orphanet:53697)
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HYPOPHOSPHATEMIC BONE DISEASE
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(OMIM:146350)
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HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE
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(OMIM:300554)
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Hereditary hypophosphatemic rickets with hypercalciuria
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(Orphanet:157215)
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Hypocalcemic vitamin D-dependent rickets
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(Orphanet:289157)
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Hypocalcemic vitamin D-resistant rickets
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(Orphanet:93160)
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Hypophosphatemic rickets, autosomal recessive, 2
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(OMIM:613312)
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METAPHYSEAL ANADYSPLASIA 2
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(OMIM:613073)
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Mesomelic dwarfism - cleft palate - camptodactyly
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(Orphanet:2631)
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Metaphyseal dysostosis - intellectual deficit - conductive deafness
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(Orphanet:2502)
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OSTEOGENESIS IMPERFECTA, TYPE VII
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(OMIM:610682)
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Perinatal lethal hypophosphatasia
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(Orphanet:247623)
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Short rib-polydactyly syndrome, Beemer-Langer type
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(Orphanet:93268)
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Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification
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(Orphanet:93358)
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Spondyloepimetaphyseal dysplasia, Pakistani type
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(Orphanet:93282)
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Spondyloepimetaphyseal dysplasia, matrilin-3 type
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(Orphanet:156728)
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TIBIAL TORSION, BILATERAL MEDIAL
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(OMIM:188800)
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VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A
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(OMIM:264700)
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VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B
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(OMIM:600081)
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VITAMIN D-DEPENDENT RICKETS, TYPE 2A
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(OMIM:277440)
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VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR
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(OMIM:600785)
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X-linked hypophosphatemia
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(Orphanet:89936)
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