ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2
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(OMIM:614473)
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Arterial calcification, generalized, of infancy, 1
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(OMIM:208000)
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Autosomal dominant hypophosphatemic rickets
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(Orphanet:89937)
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Autosomal recessive hypophosphatemic rickets
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(Orphanet:289176)
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CYSTINOSIS, NEPHROPATHIC
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(OMIM:219800)
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Generalized arterial calcification of infancy
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(Orphanet:51608)
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HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM
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(OMIM:612089)
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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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Hypophosphatemic rickets, autosomal recessive, 2
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(OMIM:613312)
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Linear nevus sebaceus syndrome
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(Orphanet:2612)
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Tyrosinemia type 1
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(Orphanet:882)
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X-linked hypophosphatemia
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(Orphanet:89936)
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