Autosomal recessive spastic paraplegia type 23 (Q99390): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Paraplegia espástica progressiva associada ao fenótipo SPG23, caracterizada por neuropatia periférica, anormalidades na pigmentação da pele, cabelos prematuramente grisalhos e características faciais típicas.
@@ description / en / description / en @@
+Progressive spastic paraplegia associated with the SPG23 phenotype that is characterized by by peripheral neuropathy, skin pigment abnormalities, premature graying of hair and characteristic facial features.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1595722974
@@ Property / Canonical URI: https://id.who.int/icd/entity/1595722974 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_1595722974
@@ Property / CURIE: CID11:ID_1595722974 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_1595722974
@@ Property / Canary Token: dki-india-ID_1595722974 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-15T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 15 August 2026 / rank @@
+Normal rank

Latest revision as of 16:03, 16 August 2026

Progressive spastic paraplegia associated with the SPG23 phenotype that is characterized by by peripheral neuropathy, skin pigment abnormalities, premature graying of hair and characteristic facial features.

Language	Label	Description	Also known as
default for all languages	ID_1595722974
English	Autosomal recessive spastic paraplegia type 23	Progressive spastic paraplegia associated with the SPG23 phenotype that is characterized by by peripheral neuropathy, skin pigment abnormalities, premature graying of hair and characteristic facial features.