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bn:01227149n
Noun Concept
Categories: Autosomal dominant disorders, Syndromes affecting teeth, Syndromes affecting head size, Syndromes affecting stature, Rare syndromes
EN
Langer–Giedion syndrome  trichorhinophalangeal syndrome type II  Chromosome 8Q24.1 Deletion Syndrome  Deletion 8q24.1  Langer-Giedion chromosome region
EN
Langer–Giedion syndrome is a very uncommon autosomal dominant genetic disorder caused by a deletion of a small section of material on chromosome 8. Wikipedia
Definitions
Relations
Sources
EN
Langer–Giedion syndrome is a very uncommon autosomal dominant genetic disorder caused by a deletion of a small section of material on chromosome 8. Wikipedia
Human disease Wikidata
IS A
syndrome
Tricho–rhino–phalangeal syndrome
GENETIC ASSOCIATION
Tricho-rhino-phalangeal syndrome Type 1
EXT1
HEALTH SPECIALTY
medical genetics
SYMPTOMS
shortness
Wikipedia
EN
Langer–Giedion syndrome
Wikidata
EN
trichorhinophalangeal syndrome type II
Wikipedia Redirections
EN
Langer-Giedion chromosome region, Langer-Giedion syndrome, Langer-giedion syndrome, LGCR
Wikidata Alias
EN
Chromosome 8Q24.1 Deletion Syndrome, Deletion 8q24.1, Langer-Giedion syndrome, Monosomy 8q24.1, Trichorhinophalangeal dysplasia type II, TRICHORHINOPHALANGEAL SYNDROME, TYPE II, TRICHORHINOPHALANGEAL SYNDROME, TYPE II; TRPS2, Trichorhinophalangeal syndrome type 2, TRPS2

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