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Descriptor English: Nail-Patella Syndrome
Descriptor Spanish: Síndrome de la Uña-Rótula
Descriptor síndrome uña-rótula
Entry term(s) onicosteodisplasia hereditaria
síndrome de Osterreicher
síndrome de Tuner-Kieser
síndrome del cuerno iliaco
síndrome del cuerno pélvico
síndrome onicorrotuliano
Scope note: Síndrome de alteraciones múltiples que se caracteriza por ausencia o hipoplasia de la RÓTULA y distrofia congénita de las uñas. Es un síndrome genético, determinado por un rasgo autosómico dominante.
Descriptor Portuguese: Síndrome da Unha-Patela
Descriptor French: Syndrome nail-patella
Entry term(s): Disease, Fong
Fong Disease
Hereditary Onycho-Osteodysplasia
Hereditary Osteo-Onychodysplasia
Hereditary Osteo-Onychodysplasias
Nail Patella Syndrome
Onychoosteodysplasia
Osteo Onychodysplasia, Hereditary
Osteo-Onychodysplasia, Hereditary
Osteo-Onychodysplasias, Hereditary
Osterreicher Syndrome
Pelvic Horn Syndrome
Syndrome, Nail-Patella
Syndrome, Osterreicher
Syndrome, Pelvic Horn
Syndrome, Turner-Kieser
Turner Kieser Syndrome
Turner-Kieser Syndrome
Tree number(s): C05.550.629
C16.131.077.606
C16.320.600
C17.800.529.400
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D009261
Scope note: 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.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Public MeSH Note: 65
History Note: 65(63)
DeCS ID: 9452
Unique ID: D009261
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1965/01/01
Date of Entry: 1999/01/01
Revision Date: 2013/07/08
Nail-Patella Syndrome - Preferred
Concept UI M0014428
Scope note 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.
Preferred term Nail-Patella Syndrome
Entry term(s) Disease, Fong
Fong Disease
Hereditary Onycho-Osteodysplasia
Hereditary Osteo-Onychodysplasia
Hereditary Osteo-Onychodysplasias
Nail Patella Syndrome
Onychoosteodysplasia
Osteo Onychodysplasia, Hereditary
Osteo-Onychodysplasia, Hereditary
Osteo-Onychodysplasias, Hereditary
Osterreicher Syndrome
Pelvic Horn Syndrome
Syndrome, Nail-Patella
Syndrome, Osterreicher
Syndrome, Pelvic Horn
Syndrome, Turner-Kieser
Turner Kieser Syndrome
Turner-Kieser Syndrome



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