Hypoplasia of the radius

Symptom Information:

Symptom ID: HPO:0002984
Synonyms:
Hypoplastic radii [HPO:0002984]
Hypoplastic radius [HPO:0002984]
Radial hypoplasia [HPO:0002984]
Radial ray hypoplasia [HPO:0002984]
Short radii [HPO:0002984]
Short radius [HPO:0002984]
Shortening of radius [HPO:0002984]
Radius hypoplasia [Orphanet:19240]
Hypoplasia of radius [HPO:0002984]
Hypoplasia of radius (disorder) [Orphanet:19240]
Partial radial absence (disorder) [Orphanet:19240]
Congenital hypoplasia of radius (disorder) [Orphanet:19240]
Partial radial absence [Orphanet:19240]
Congenital hypoplasia of radius [Orphanet:19240]
Hypoplastic radii [OMIM:Hypoplastic radii]
Hypoplastic radius [OMIM:Hypoplastic radius]
Radial hypoplasia [OMIM:Radial hypoplasia]
Radial ray hypoplasia [OMIM:Radial ray hypoplasia]
Short radii [OMIM:Short radii]
Short radius [OMIM:Short radius]
short radii [OMIM:short radii]
Radius anomaly/absence/agenesis/hypoplasia/abnormal radial ray [Orphanet:19240]
Radial hypoplasia (1 patient) [OMIM:Radial hypoplasia (1 patient)]
Quality:
Cross references:
HPO:0006501 "Aplasia/Hypoplasia of the radius" [Orphanet:19240]
Orphanet:19240 "Radius anomaly/absence/agenesis/hypoplasia/abnormal radial ray" [Orphanet:19240]
OMIM: "Hypoplastic radii" [OMIM:Hypoplastic radii]
OMIM: "Hypoplastic radius" [OMIM:Hypoplastic radius]
OMIM: "Radial hypoplasia" [OMIM:Radial hypoplasia]
OMIM: "Radial ray hypoplasia" [OMIM:Radial ray hypoplasia]
OMIM: "Short radii" [OMIM:Short radii]
OMIM: "Short radius" [OMIM:Short radius]
OMIM: "short radii" [OMIM:short radii]
OMIM: "Radial hypoplasia (1 patient)" [OMIM:Radial hypoplasia (1 patient)]
UMLS:C0431843 "Partial radial absence" [Orphanet:19240]
UMLS:C0685381 "Congenital hypoplasia of radius" [Orphanet:19240]
Is a (Direct Parents):
Orphanet Abnormality of the radius
Orphanet Upper limb segmental anomalies
HPO         Aplasia/Hypoplasia of the radius
HPO         Forearm undergrowth
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Aplasia/hypoplasia of the extremities(HPO:0009815)
                      Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                         Aplasia/hypoplasia involving forearm bones(HPO:0006503)
                            Aplasia/Hypoplasia of the radius(HPO:0006501)
                               Hypoplasia of the radius(HPO:0002984)
                            Forearm undergrowth(HPO:0009821)
                               Hypoplasia of the radius(HPO:0002984)
                      Limb undergrowth(HPO:0009826)
                         Forearm undergrowth(HPO:0009821)
                            Hypoplasia of the radius(HPO:0002984)
                   Abnormality of the upper limb(HPO:0002817)
                      Abnormality of the forearm(HPO:0002973)
                         Abnormality of the radius(HPO:0002818)
                            Aplasia/Hypoplasia of the radius(HPO:0006501)
                               Hypoplasia of the radius(HPO:0002984)
                         Aplasia/hypoplasia involving forearm bones(HPO:0006503)
                            Aplasia/Hypoplasia of the radius(HPO:0006501)
                               Hypoplasia of the radius(HPO:0002984)
                            Forearm undergrowth(HPO:0009821)
                               Hypoplasia of the radius(HPO:0002984)
                      Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                         Aplasia/hypoplasia involving forearm bones(HPO:0006503)
                            Aplasia/Hypoplasia of the radius(HPO:0006501)
                               Hypoplasia of the radius(HPO:0002984)
                            Forearm undergrowth(HPO:0009821)
                               Hypoplasia of the radius(HPO:0002984)
             Abnormality of long bone morphology(HPO:0011314)
                Short long bone(HPO:0003026)
                   Forearm undergrowth(HPO:0009821)
                      Hypoplasia of the radius(HPO:0002984)
             Aplasia/hypoplasia involving the skeleton(HPO:0009115)
                Aplasia/hypoplasia of the extremities(HPO:0009815)
                   Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                      Aplasia/hypoplasia involving forearm bones(HPO:0006503)
                         Aplasia/Hypoplasia of the radius(HPO:0006501)
                            Hypoplasia of the radius(HPO:0002984)
                         Forearm undergrowth(HPO:0009821)
                            Hypoplasia of the radius(HPO:0002984)
                   Limb undergrowth(HPO:0009826)
                      Forearm undergrowth(HPO:0009821)
                         Hypoplasia of the radius(HPO:0002984)
MedDRA:
Database Frequency: 44 / 7739
Resource:

All diseases associated with this symptom:

ARMS, MALFORMATION OF (OMIM:107900)
Achondrogenesis (Orphanet:932)
Achondrogenesis type 1A (Orphanet:93299)
Acro-renal-mandibular syndrome (Orphanet:958)
Acro-renal-ocular syndrome (Orphanet:959)
Acrocapitofemoral dysplasia (Orphanet:63446)
Acromesomelic dysplasia, Grebe type (Orphanet:2098)
Acromesomelic dysplasia, Hunter-Thomson type (Orphanet:968)
Acromesomelic dysplasia, Maroteaux type (Orphanet:40)
BRACHYMESOMELIA-RENAL SYNDROME (OMIM:113470)
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
Baller-Gerold syndrome (Orphanet:1225)
Blackfan-Diamond anemia (Orphanet:124)
Brachydactyly type A6 (Orphanet:93382)
Cenani-Lenz syndrome (Orphanet:3258)
Cornelia de Lange syndrome (Orphanet:199)
DIAMOND-BLACKFAN ANEMIA 11 (OMIM:614900)
FANCONI ANEMIA, COMPLEMENTATION GROUP O (OMIM:613390)
FANCONI ANEMIA, COMPLEMENTATION GROUP P (OMIM:613951)
Fuhrmann syndrome (Orphanet:2854)
Holoprosencephaly - radial heart renal anomalies (Orphanet:3186)
Holt-Oram syndrome (Orphanet:392)
IVIC syndrome (Orphanet:2307)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Langer mesomelic dysplasia (Orphanet:2632)
Lethal chondrodysplasia, Seller type (Orphanet:1421)
Lethal faciocardiomelic dysplasia (Orphanet:1972)
Léri-Weill dyschondrosteosis (Orphanet:240)
MESOMELIC DWARFISM OF HYPOPLASTIC TIBIA AND RADIUS TYPE (OMIM:156230)
Microgastria - limb reduction defect (Orphanet:2538)
Nager syndrome (Orphanet:245)
Okihiro syndrome (Orphanet:93293)
Phocomelia, Schinzel type (Orphanet:2879)
Postaxial acrofacial dysostosis (Orphanet:246)
Radial hypoplasia - triphalangeal thumbs - hypospadias - maxillary diastema (Orphanet:2252)
Radial ray hypoplasia - choanal atresia (Orphanet:3026)
Richieri Costa-Pereira syndrome (Orphanet:3102)
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL (OMIM:602613)
TARP syndrome (Orphanet:2886)
Ulbright-Hodes syndrome (Orphanet:3404)
Ulnar-mammary syndrome (Orphanet:3138)
Upper limb mesomelic dysplasia (Orphanet:2497)
VACTERL/VATER association (Orphanet:887)
WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME (OMIM:602418)