Autosomal recessive ataxia with oculomotor apraxia type 2 (Q96462): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Ataxia-apraxia oculomotora tipo 2 é uma forma de ataxia cerebelar autossômica recessiva caracterizada por ataxia cerebelar progressiva, neuropatia sensitivo-motora axonal com apraxia oculomotora, instabilidade de fixação, características extrapiramidais e um nível elevado de alfa-fetoproteína sérica.
@@ description / en / description / en @@
+Ataxia-oculomotor apraxia type 2 is a form of autosomal recessive cerebellar ataxia characterised by progressive cerebellar ataxia, axonal sensorimotor neuropathy with oculomotor apraxia, fixation instability, extrapyramidal features and an elevated serum alpha-fetoprotein level.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/907196820
@@ Property / Canonical URI: https://id.who.int/icd/entity/907196820 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_907196820
@@ Property / CURIE: CID11:ID_907196820 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_907196820
@@ Property / Canary Token: dki-india-ID_907196820 / 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 12:28, 16 August 2026

Ataxia-oculomotor apraxia type 2 is a form of autosomal recessive cerebellar ataxia characterised by progressive cerebellar ataxia, axonal sensorimotor neuropathy with oculomotor apraxia, fixation instability, extrapyramidal features and an elevated serum alpha-fetoprotein level.

Language	Label	Description	Also known as
default for all languages	ID_907196820
English	Autosomal recessive ataxia with oculomotor apraxia type 2	Ataxia-oculomotor apraxia type 2 is a form of autosomal recessive cerebellar ataxia characterised by progressive cerebellar ataxia, axonal sensorimotor neuropathy with oculomotor apraxia, fixation instability, extrapyramidal features and an elevated serum alpha-fetoprotein level.