Disease #02698 (CMT1F (Charcot-Marie-Tooth disease, type IF (CMT-1F)), OMIM:607734)

Official abbreviation CMT1F
Name Charcot-Marie-Tooth disease, type IF (CMT-1F)
OMIM ID 607734
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 1
Associated with 1 gene NEFL
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00228245 - - - - - - - - - - - CMT1F - NEFL NEFL 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00375207 - - - - - - - - - - - CMT1F - NEFL NEFL 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00397517 Pat5 PubMed: Horga 2017 2-generation family, 1 affected, unaffected parents M no United Kingdom (Great Britain) Brittish >76y - - - CMT1F see paper; unsteady gait (HP:0002317), tremor hands (HP:0002378), muscle atrophy hands (HP:0008948), lower limb muscular atrophy (HP:0008944), upper limb muscle weakness (HP:0003484), lower limb muscle weakness (HP:0007340); no deep tendon reflexes (HP:0001284), pinprick sensation reduced to above ankles (HP:0007328), vibration sense reduced to knees (HP:0002495), position sense reduced to ankles (HP:0002070), no pyramidal signs (-HP:0007256), positive Romberg sign (HP:0002403), stamping gait, ataxic gait (HP:0002066), no pes cavus (-HP:0001761); mild head tremor (HP:0002346), thickened ulnar nerve; neuropathy with axonal and demyelinating features (HP:0009830); MRI brain normal; MRI spinal cord normal, ... NEFL NEFL 1 1 Farina Kemper
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