Disease #01089 (SPG30 (paraplegia, spastic, type 30, autosomal recessive), OMIM:610357)

Official abbreviation SPG30
Name paraplegia, spastic, type 30, autosomal recessive
OMIM ID 610357
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 5
Phenotype entries for this disease 2
Associated with 1 gene KIF1A
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2022-01-18 16:00:52 +01:00 (CET)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00054877 Pat22 PubMed: van de Warrenburg 2016, Journal: van de Warrenburg 2016 - M - - - - - - - SPG30 - KIF1A KIF1A 1 1 Erik-Jan Kamsteeg
00306152 - - - M no Russian Federation - - - - - SPG30 Phenotype at the examination: body mass 40 kg (>97 centile), height 130 cm (>95 centile), body mass index 100 centile, head circumference 54 cm, facial features prominent incisors, poor dermatoglyphics; tendon reflexes are brisk (in legs more than in arms), gait was slow, spastic with elements paretic and leg recurvation; mental retardation (MR), quiet behavior, stereotypies. KIF1A KIF1A 1 1 Varvara Kadnikova
00306153 - - - M - Russian Federation - - - - - SPG30 - KIF1A KIF1A 1 1 Varvara Kadnikova
00306154 - - - M - Russian Federation - - - - - SPG30 - KIF1A KIF1A 1 1 Varvara Kadnikova
00306155 - - - F - Russian Federation - - - - - SPG30 - KIF1A KIF1A 1 1 Varvara Kadnikova
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