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  • hereditary fragility of bone
    À¯Àü¼º °ñÃë¾àÁõ (¡­Íéöªå°ñø).
  • hereditary fructose intolerance
    À¯Àü¼º ÇÁ·èÅä¿À½º ºÒ³»Áõ(¡­ÝÕÒ±ñø).
  • hereditary glycinuria
    À¯Àü¼º ±Û¸®½Å´¢Áõ.
  • hereditary hemorhagic telangiectasia(osler-weber-rendu disease,)
    À¯Àü¼ºÃâÇ÷¼º¸ð¼¼Ç÷°ü È®Àå
  • hereditary hemorrhagic angioma
    À¯Àü(¼º) ÃâÇ÷¼º Ç÷°üÁ¾.
  • hereditary hemorrhagic telangiectasia
    À¯Àü(¼º) ÃâÇ÷¼º ¸ð¼¼(Ç÷)°üÈ®Àå.
  • hereditary hemorrhagic telangiectasia
    À¯Àü¼º ÃâÇ÷ Ç÷°üÈ®Àå
  • hereditary hyposegmentation
    À¯Àü¼º ÀúºÐ ÀýÁõ.
  • hereditary labyrinthine deafness
    À¯Àü¼º ³»À̼º ³­Ã»(¡­Ò®ì¼àõÑñôé).
  • hereditary labyrinthine deafness
    À¯Àü¼º ³»À̼º ³­Ã»
  • hereditary leptocytosis
    À¯Àü¼º Ç¥ÀûÀûÇ÷±¸ Áõ°¡(Áõ).
  • hereditary lymphedema
    À¯Àü¼º¸²ÇÁºÎÁ¾
  • hereditary macular degeneration
    À¯Àü¼º Ȳ¹Ýº¯¼º(ë¶îîàõüÜÚèܨàõ).
  • hereditary macular dystrophy
    À¯Àü¼ºÈ²¹ÝÀÌ¿µ¾ç(Áõ)
  • hereditary methemoglobinemia
    À¯Àü¼º ¸ÞÆ®Çì¸ð±Û·ÎºóÇ÷Áõ.
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  • hereditary optic atrophy
    À¯Àü¼º½Ã½Å°æÀ§Ãà.
  • hereditary oral mucoepithelial dysplasia
    À¯Àü¼º ±¸°­ Á¡¸· »óÇÇ ÀÌÇü¼º
  • hereditary orotic aciduria
    À¯Àü¼º ¿À·Îƾ»ê´¢Áõ.
  • hereditary osteodystrophy
    À¯Àü¼º °ñ ÀÌ¿µ¾çÁõ
  • hereditary persistence of Hb F =HPFH
    À¯Àü¼º žÆÇ÷»ö¼ÒÁö¼Óº´(Áõ)
  • hereditary plamoplantar keratoderma
    À¯Àü¼º ¼Õ¹ß¹Ù´Ú°¢ÇÇÁõ
  • hereditary porphyria
    À¯Àü¼º Æ÷¸£ÇǸ°Áõ.
  • hereditary porphyria cutanea tarda
    À¯Àü¼º ¸¸¹ß¼º ÇǺΠÆ÷¸£ÇǸ°Áõ
  • hereditary progressive mucinous histiocytosis X
    À¯Àü¼º ÁøÇ༺ Á¡¾×¼ºÁ¶Á÷±¸Áõ
  • hereditary protocoproporphyria
    À¯Àü¼º ÇÁ·ÎÅäÄÚÇÁ·ÎÆ÷¸£ÇǸ°Áõ
  • hereditary pyloric stenosis
    À¯Àü¼º À¯¹®ÇùÂøÁõ(¡­êëÚ¦úõó¸ñø).
  • hereditary pyloric stenosis
    À¯Àü¼º À¯¹®ÇùÂøÁõ(¡­À¯¹®ÇùÂøÁõ).
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  • hereditary sclerosing poikiloderma
    À¯Àü¼º °æÈ­¼º ´ÙÇüÇǺÎÁõ
  • hereditary spastic paraplegia
    À¯Àü¼º ¿¬Ã༺ ´ë¸¶ºñ.
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RFP recurrent facial paralysis; request for proposal; right frontoposterior [fetal position]
AHC Albright's Hereditary Osteodystrophy
AHO Albright's Hereditary Osteodystrophy
HCP Hereditary Copro-Porphyria; À¯Àü¼º CoproPorphyria
HEMPAS Test Hereditary Erythrocytic Multinuclearity with Positive Acidified Serum Test
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HT1 Hereditary Tyrosinemia Type I
HAE Hereditary angioneurotic edema
HCHWA-D Hereditary cerebral haemorrhage with amyloidosis, Dutch type
HCP Hereditary coproporphyria
HH Hereditary haemochromatosis
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glossolabiolaryngeal paralysis Progressive weakness and atrophy of the muscles of the tongue, lips, palate, pharynx, and larynx, usually occurring in later life; most often caused by motor neuron disease.
Synonym: bulbar palsy, bulbar paralysis, Duchenne's disease, Erb disease, glossolabiolaryngeal paralysis, glossolabiopharyngeal paralysis.
(05 Mar 2000)
glossopalatolabial paralysis One of the subgroups of motor neuron disease; a progressive degenerative disorder of the motor neurons of primarily the brainstem, manifested as weakness (and wasting) of the various bulbar muscles, resulting in dysarthria and dysphagia-fluid regurgitation is an outstanding symptom and can cause aspiration; tongue weakness and wasting is usually evident, and often the fasciculation potentials are present in the tongue and facial muscles.
Synonym: glossopalatolabial paralysis, glossopharyngeolabial paralysis.
(05 Mar 2000)
glossopharyngeolabial paralysis One of the subgroups of motor neuron disease; a progressive degenerative disorder of the motor neurons of primarily the brainstem, manifested as weakness (and wasting) of the various bulbar muscles, resulting in dysarthria and dysphagia-fluid regurgitation is an outstanding symptom and can cause aspiration; tongue weakness and wasting is usually evident, and often the fasciculation potentials are present in the tongue and facial muscles.
Synonym: glossopalatolabial paralysis, glossopharyngeolabial paralysis.
(05 Mar 2000)
vocal cord paralysis Paralysis of one or both of the vocal cords.
(12 Dec 1998)
central paralysis Paralysis due to a lesion in the brain or spinal cord.
(05 Mar 2000)
Chastek paralysis A disease of foxes and mink caused by feeding on raw fish of certain types which contain an enzyme destructive of thiamin; the thiamin deficiency causes loss of appetite, emaciation, and finally paralysis and death.
(05 Mar 2000)
periodic paralysis Term for a group of diseases characterised by recurring episodes of muscular weakness or flaccid paralysis without loss of consciousness, speech, or sensation; attacks begin when the patient is at rest, and there is apparent good health between attacks.
See: hyperkalaemic periodic paralysis, hypokalaemic periodic paralysis, normokalaemic periodic paralysis.
(05 Mar 2000)
peripheral facial paralysis A condition that involves the facial nerve (VII cranial nerve) and results in the paralysis of one side of the face. Bell's (facial nerve palsy) can be differentiated from a central (stroke) deficit by the inability to raise the eyebrow on the affected side.
(27 Sep 1997)
Gubler's paralysis <syndrome> A form of alternating hemiplegia characterised by contralateral hemiplegia and ipsilateral facial paralysis.
Synonym: Gubler's paralysis, Millard-Gubler syndrome.
(05 Mar 2000)
mimetic paralysis Paralysis of the facial muscles.
(05 Mar 2000)
mixed paralysis Combined motor and sensory paralysis.
(05 Mar 2000)
wasting paralysis A serious neurologic disease that results from the progressive degeneration of the motor neurons.
(27 Sep 1997)
motor paralysis Loss of the power of muscular contraction.
(05 Mar 2000)
compression paralysis Paralysis due to external presure on a nerve.
(05 Mar 2000)
musculospiral paralysis Paralysis of the muscles of the forearm due to injury of the radial (musculospiral) nerve.
(05 Mar 2000)
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