Osteolytic defects of the phalanges of the hand
All diseases associated with this symptom:
Acro-osteolysis-keloid-like lesions-premature aging syndrome
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(Orphanet:363665)
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Acroosteolysis, dominant type
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(Orphanet:955)
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Cranio-osteoarthropathy
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(Orphanet:1525)
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Diffuse cutaneous systemic sclerosis
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(Orphanet:220393)
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Ehlers-Danlos syndrome, vascular type
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(Orphanet:286)
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HAJDU-CHENEY SYNDROME
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(OMIM:102500)
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Haim-Munk syndrome
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(Orphanet:2342)
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Hereditary sensory and autonomic neuropathy type 2
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(Orphanet:970)
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Limited cutaneous systemic sclerosis
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(Orphanet:220402)
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NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA
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(OMIM:201300)
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NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB
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(OMIM:613115)
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NEUROPATHY, HEREDITARY SENSORY, TYPE IF
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(OMIM:615632)
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Necrotizing encephalomyelopathy, subacute, of Leigh, adult
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(OMIM:161700)
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Osteodysplasty, Melnick-Needles type
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(Orphanet:2484)
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SATOYOSHI SYNDROME
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(OMIM:600705)
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Singleton-Merten dysplasia
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(Orphanet:85191)
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VAN BOGAERT-HOZAY SYNDROME
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(OMIM:277150)
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