Slender long bone
Symptom Information:
Symptom ID: | HPO:0003100 | |||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |