Spondylometaphyseal dysplasia - cone-rod dystrophy (Q63005): Difference between revisions

← Older edit

@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/430156722
@@ Property / Canonical URI: https://id.who.int/icd/entity/430156722 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_430156722
@@ Property / CURIE: CID11:ID_430156722 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_430156722
@@ Property / Canary Token: dki-india-ID_430156722 / 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 +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-13T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank

Latest revision as of 10:29, 14 August 2026

Spondylometaphyseal dysplasia - cone-rod dystrophy syndrome is characterised by the association of spondylometaphyseal dysplasia (marked by platyspondyly, shortening of the tubular bones and progressive metaphyseal irregularity and cupping), with postnatal growth retardation and progressive visual impairment due to cone-rod dystrophy.

Language	Label	Description	Also known as
default for all languages	ID_430156722
English	Spondylometaphyseal dysplasia - cone-rod dystrophy	Spondylometaphyseal dysplasia - cone-rod dystrophy syndrome is characterised by the association of spondylometaphyseal dysplasia (marked by platyspondyly, shortening of the tubular bones and progressive metaphyseal irregularity and cupping), with postnatal growth retardation and progressive visual impairment due to cone-rod dystrophy.