Disease #04047 (SPG64 (paraplegia, spastic, type 64, autosomal recessive (SPG-64)), OMIM:615683)

Official abbreviation SPG64
Name paraplegia, spastic, type 64, autosomal recessive (SPG-64)
OMIM ID 615683
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene ENTPD1
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

2 entries on 1 page. Showing entries 1 - 2.
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00081212 - PubMed: Novarino 2014, Journal: Novarino 2014 4-generation family, 2 affecteds (F, M), unaffected heterozygous carrier parents, patient 1242-IV-2 M yes - - - - - - SPG64 Spasticity (HP:0001257) Talipes equinovarus (HP:0001762) Hyperreflexia (HP:0001347) Babinski sign (HP:0003487) Skeletal muscle atrophy (HP:0003202) Aggressive behavior (HP:0000718) Delayed puberty (HP:0000823) Microcephaly (HP:0000252) Intellectual disability, borderline (HP:0006889) ENTPD1 ENTPD1 1 1 Wietske Wesseling
00081221 - PubMed: Novarino 2014, Journal: Novarino 2014 patient 1242-IV-4 M yes - - - - - - SPG64 spasticity (HP:0001257), hyperreflexia (HP:0001347), Babinski sign (HP:0003487), intellectual disability, borderline (HP:0006889), delayed puberty (HP:0000823), microcephaly (HP:0000252) ENTPD1 ENTPD1 1 1 Wietske Wesseling
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