Langer-Giedion syndrome (Q46620): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A síndrome de Langer-Giedon ou síndrome tricorrinofalangiana tipo 2 é uma síndrome de anomalia cromossômica caracterizada pela associação de déficit intelectual e inúmeras outras anomalias, incluindo pele redundante, múltiplas exostoses cartilaginosas, fácies características e epífises falangianas em forma de cone.
@@ description / en / description / en @@
+Langer-Giedion syndrome or trichorhinophalangeal syndrome type 2 is a chromosomal anomaly syndrome characterised by the association of intellectual deficit and numerous other anomalies including redundant skin, multiple cartilaginous exostoses, characteristic facies and cone-shaped phalangeal epiphyses.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/315453775
@@ Property / Canonical URI: https://id.who.int/icd/entity/315453775 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:LD24.80
@@ Property / CURIE: CID11:LD24.80 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-LD24.80
@@ Property / Canary Token: dki-india-LD24.80 / 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
@@ Property / Linked ICD 10 @@
+ICD I391
@@ Property / Linked ICD 10: ICD I391 / rank @@
+Normal rank

Latest revision as of 15:19, 13 August 2026

Langer-Giedion syndrome or trichorhinophalangeal syndrome type 2 is a chromosomal anomaly syndrome characterised by the association of intellectual deficit and numerous other anomalies including redundant skin, multiple cartilaginous exostoses, characteristic facies and cone-shaped phalangeal epiphyses.

Language	Label	Description	Also known as
default for all languages	LD24.80
English	Langer-Giedion syndrome	Langer-Giedion syndrome or trichorhinophalangeal syndrome type 2 is a chromosomal anomaly syndrome characterised by the association of intellectual deficit and numerous other anomalies including redundant skin, multiple cartilaginous exostoses, characteristic facies and cone-shaped phalangeal epiphyses.