Slender long bone

Symptom Information:

Symptom ID: HPO:0003100
Synonyms:
Gracile long bones [HPO:0003100]
Long bones slender [HPO:0003100]
SLENDER LONG BONES [HPO:0003100]
Slender, gracile long tubular bones [HPO:0003100]
Thin gracile long bones [HPO:0003100]
Thin long bones [HPO:0003100]
Thin, gracile long bones [HPO:0003100]
Narrow diaphysis [Orphanet:45900]
Narrowing of bone (finding) [Orphanet:45900]
Narrowing of bone [Orphanet:45900]
Gracile long bones [OMIM:Gracile long bones]
Slender long bones [OMIM:Slender long bones]
Slender, gracile long tubular bones [OMIM:Slender, gracile long tubular bones]
Thin gracile long bones [OMIM:Thin gracile long bones]
Thin long bones [OMIM:Thin long bones]
Thin, gracile long bones [OMIM:Thin, gracile long bones]
Narrowed/gracile diaphysis/diaphyses/long bones/dolichostenomelia [Orphanet:45900]
Quality:
Cross references:
Orphanet:45900 "Narrowed/gracile diaphysis/diaphyses/long bones/dolichostenomelia" [Orphanet:45900]
OMIM: "Gracile long bones" [OMIM:Gracile long bones]
OMIM: "Slender long bones" [OMIM:Slender long bones]
OMIM: "Slender, gracile long tubular bones" [OMIM:Slender, gracile long tubular bones]
OMIM: "Thin gracile long bones" [OMIM:Thin gracile long bones]
OMIM: "Thin long bones" [OMIM:Thin long bones]
OMIM: "Thin, gracile long bones" [OMIM:Thin, gracile long bones]
UMLS:C0575132 "Narrowing of bone" [Orphanet:45900]
Is a (Direct Parents):
HPO         Slender radius
HPO         Abnormality of long bone morphology
Orphanet Abnormal diaphysis morphology
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)
             Abnormality of long bone morphology(HPO:0011314)
                Slender long bone(HPO:0003100)
MedDRA:
Database Frequency: 45 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
3M syndrome (Orphanet:2616)
Acro-osteolysis-keloid-like lesions-premature aging syndrome (Orphanet:363665)
Autosomal recessive Kenny-Caffey syndrome (Orphanet:93324)
CEREBELLOFACIODENTAL SYNDROME (OMIM:616202)
CEREBROOCULOFACIOSKELETAL SYNDROME 4 (OMIM:610758)
Camptodactyly syndrome, Guadalajara type 2 (Orphanet:1326)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Duchenne and Becker muscular dystrophy (Orphanet:262)
Ear-patella-short stature syndrome (Orphanet:2554)
FACIOCARDIOMELIC SYNDROME (OMIM:612731)
FETAL AKINESIA DEFORMATION SEQUENCE (OMIM:208150)
Fetal akinesia deformation sequence (Orphanet:994)
Hallermann-Streiff syndrome (Orphanet:2108)
Lethal congenital contracture syndrome type 1 (Orphanet:1486)
MEIER-GORLIN SYNDROME 1 (OMIM:224690)
MEIER-GORLIN SYNDROME 2 (OMIM:613800)
MEIER-GORLIN SYNDROME 3 (OMIM:613803)
MEIER-GORLIN SYNDROME 4 (OMIM:613804)
MEIER-GORLIN SYNDROME 5 (OMIM:613805)
MGAT2-CDG (Orphanet:79329)
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III (OMIM:210730)
Marshall-Smith syndrome (Orphanet:561)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Mulibrey nanism (Orphanet:2576)
Multicentric carpo-tarsal osteolysis with or without nephropathy (Orphanet:2774)
Multiple endocrine neoplasia type 2 (Orphanet:653)
Neurofibromatosis type 1 (Orphanet:636)
OSTEOGENESIS IMPERFECTA, TYPE III (OMIM:259420)
OSTEOGENESIS IMPERFECTA, TYPE VIII (OMIM:610915)
Osteocraniostenosis (Orphanet:2763)
Osteogenesis imperfecta (Orphanet:666)
Osteogenesis imperfecta type 3 (Orphanet:216812)
Pelvic dysplasia - arthrogryposis of lower limbs (Orphanet:2840)
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL (OMIM:602613)
Short rib-polydactyly syndrome (Orphanet:1505)
Spinocerebellar ataxia - dysmorphism (Orphanet:1185)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
THREE M SYNDROME 2 (OMIM:612921)
THREE M SYNDROME 3 (OMIM:614205)
Teebi-Shaltout syndrome (Orphanet:3291)
Tel Hashomer camptodactyly syndrome (Orphanet:3292)
Thin ribs - tubular bones - dysmorphism (Orphanet:1506)
Van den Ende-Gupta syndrome (Orphanet:2460)
Wrinkly skin syndrome (Orphanet:2834)