Concept information
Preferred term
Nail-Patella Syndrome
Type
-
mesh:Descriptor
Definition
- A syndrome of multiple abnormalities characterized by the absence or hypoplasia of the PATELLA and congenital nail dystrophy. It is a genetically determined autosomal dominant trait.
Broader concept
Entry terms
- Fong Disease
- Hereditary Onycho-Osteodysplasia
- Hereditary Osteo-Onychodysplasias
- Onychoosteodysplasia
- Osteo-Onychodysplasia, Hereditary
- Osterreicher Syndrome
- Pelvic Horn Syndrome
- Turner-Kieser Syndrome
Allowable Qualifier(s)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemically induced (Qualifier)
- classification (Qualifier)
- complications (Qualifier)
- diagnosis (Qualifier)
- diagnostic imaging (Qualifier)
- diet therapy (Qualifier)
- drug therapy (Qualifier)
- economics (Qualifier)
- embryology (Qualifier)
- enzymology (Qualifier)
- epidemiology (Qualifier)
- ethnology (Qualifier)
- etiology (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- metabolism (Qualifier)
- microbiology (Qualifier)
- mortality (Qualifier)
- nursing (Qualifier)
- parasitology (Qualifier)
- pathology (Qualifier)
- physiopathology (Qualifier)
- prevention & control (Qualifier)
- psychology (Qualifier)
- radiotherapy (Qualifier)
- rehabilitation (Qualifier)
- surgery (Qualifier)
- therapy (Qualifier)
- urine (Qualifier)
- veterinary (Qualifier)
- virology (Qualifier)
In other languages
-
French
-
Maladie de Fong
-
Onycho-arthro-ostéodysplasie héréditaire
-
Onycho-ostéo-dysplasie héréditaire
-
Onycho-ostéodysplasie héréditaire
-
Ostéo-onychodysostose
-
Ostéo-onychodysplasie héréditaire
-
Syndrome d'Österreicher
-
Syndrome de Turner-Kieser
URI
http://data.loterre.fr/ark:/67375/JVR-RTSHNPV7-9
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