A form of syndromic craniosynostosis with characteristics of craniosynostosis, mild facial dysmorphism (prominent supraorbital ridges, mild proptosis and maxillary hypoplasia) and calcification of the basal ganglia. The disease is associated with a f

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syndroom van Longman-Tolmie

SNOMEDCT-BE (prominent supraorbital ridges, mild proptosis and maxillary hypoplasia) and calcification of the basal ganglia. The disease is associated with a f / 720816004

SNOMEDCT-BE (disorder) / 720816004

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A rare medullar disease defined as a development of a fluid-filled cavity or syrinx within the spinal cord due to blockage of cerebrospinal fluid circulation (for example due to basal arachnoiditis, meningeal carcinomatosis, various mass lesions), sp

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secundaire syringomyelie

SNOMEDCT-BE (for example due to basal arachnoiditis, meningeal carcinomatosis, various mass lesions), sp / 770683002

SNOMEDCT-BE (disorder) / 770683002

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A rare otorhinolaryngologic disease with characteristics of the unilateral or bilateral dehiscence of the bone(s) overlying the superior (most common), lateral or posterior semicircular canal(s). Patients present audiological (autophony, aural fullne

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semicirculair kanaal-dehiscentiesyndroom

SNOMEDCT-BE (s) overlying the superior (most common), lateral or posterior semicircular canal(s). Patients present audiological (autophony, aural fullne / 768933005

SNOMEDCT-BE (disorder) / 768933005

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A rare genetic neuromuscular disease with characteristics of acute episodic muscle weakness in upper and lower extremities (which responds to acetazolamide treatment) associated with later-onset chronic slowly progressive distal axonal neuropathy.

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periodieke verlamming met distale motorneuropathie met latere aanvang

SNOMEDCT-BE (which responds to acetazolamide treatment) associated with later-onset chronic slowly progressive distal axonal neuropathy. / 774154008

SNOMEDCT-BE (disorder) / 774154008

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basal | base

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basaal | met betrekking tot een stof die zout vormt

UGENT - Medical terms -

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