Increased susceptibility to fractures
Symptom Information:
Symptom ID: | HPO:0002659 | ||||||||||||||||||||||||
Synonyms: |
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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 physiology(HPO:0011843) Increased susceptibility to fractures(HPO:0002659) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Bone disorders (excl congenital and fractures)(MedDRA:10005959) Metabolic bone disorders(MedDRA:10027425) Increased susceptibility to fractures(HPO:0002659) |
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Database Frequency: | 110 / 7739 | ||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Achondrogenesis type 1A | (Orphanet:93299) |
Acroosteolysis, dominant type | (Orphanet:955) |
Adamantinoma | (Orphanet:55881) |
Aggressive systemic mastocytosis | (Orphanet:98850) |
Albers-Schönberg osteopetrosis | (Orphanet:53) |
Albright hereditary osteodystrophy | (Orphanet:665) |
Antley-Bixler syndrome | (Orphanet:83) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Autosomal dominant hyper-IgE syndrome | (Orphanet:2314) |
Autosomal dominant hypophosphatemic rickets | (Orphanet:89937) |
Autosomal recessive cutis laxa type 1 | (Orphanet:90349) |
Autosomal recessive malignant osteopetrosis | (Orphanet:667) |
BRUCK SYNDROME 1 | (OMIM:259450) |
BRUCK SYNDROME 2 | (OMIM:609220) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Bowed tibiae - radial anomalies - osteopenia - fractures | (Orphanet:3331) |
Brittle cornea syndrome | (Orphanet:90354) |
Bruck syndrome | (Orphanet:2771) |
Buschke-Ollendorff syndrome | (Orphanet:1306) |
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
CLEIDOCRANIAL DYSPLASIA | (OMIM:119600) |
Campomelic dysplasia | (Orphanet:140) |
Classical homocystinuria | (Orphanet:394) |
Cleidocranial dysplasia | (Orphanet:1452) |
Cole-Carpenter syndrome | (Orphanet:2050) |
Congenital erythropoietic porphyria | (Orphanet:79277) |
Congenital osteogenesis imperfecta - microcephaly - cataracts | (Orphanet:2772) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Cushing syndrome due to ectopic ACTH secretion | (Orphanet:99889) |
Cutaneous mastocytosis | (Orphanet:66646) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 | (OMIM:224230) |
Dermatitis herpetiformis | (Orphanet:1656) |
Dominant hypophosphatemia with nephrolithiasis or osteoporosis | (Orphanet:244305) |
Dyskeratosis congenita | (Orphanet:1775) |
Dysosteosclerosis | (Orphanet:1782) |
Dysplasia epiphysealis hemimelica | (Orphanet:1822) |
Ehlers-Danlos syndrome, arthrochalasic type | (Orphanet:1899) |
Eosinophilic granuloma | (Orphanet:99871) |
Familial dysautonomia | (Orphanet:1764) |
Familial osteodysplasia, Anderson type | (Orphanet:2769) |
Gaucher disease | (Orphanet:355) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 3 | (Orphanet:77261) |
Geroderma osteodysplastica | (Orphanet:2078) |
Gnathodiaphyseal dysplasia | (Orphanet:53697) |
Grange syndrome | (Orphanet:79094) |
HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA | (OMIM:615267) |
HYPOGONADOTROPIC HYPOGONADISM 19 WITH OR WITHOUT ANOSMIA | (OMIM:615269) |
HYPOGONADOTROPIC HYPOGONADISM 20 WITH OR WITHOUT ANOSMIA | (OMIM:615270) |
HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA | (OMIM:615271) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
Hypophosphatasia | (Orphanet:436) |
Idiopathic juvenile osteoporosis | (Orphanet:85193) |
Juvenile Paget disease | (Orphanet:2801) |
Kallmann syndrome | (Orphanet:478) |
LOEYS-DIETZ SYNDROME 2 | (OMIM:610168) |
Lethal congenital contracture syndrome type 1 | (Orphanet:1486) |
Lethal multiple pterygium syndrome | (Orphanet:33108) |
Lichstenstein syndrome | (Orphanet:2390) |
Maffucci syndrome | (Orphanet:163634) |
Majeed syndrome | (Orphanet:77297) |
Marshall-Smith syndrome | (Orphanet:561) |
Mastocytosis | (Orphanet:98292) |
Mazabraud syndrome | (Orphanet:57782) |
McCune-Albright syndrome | (Orphanet:562) |
Menkes disease | (Orphanet:565) |
Metaphyseal dysplasia - maxillary hypoplasia - brachydacty | (Orphanet:2504) |
Microspherophakia - metaphyseal dysplasia | (Orphanet:2551) |
Mohr-Tranebjaerg syndrome | (Orphanet:52368) |
Monosomy 5p | (Orphanet:281) |
Multiple non-ossifying fibromatosis | (Orphanet:2029) |
Multiple osteochondromas | (Orphanet:321) |
NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1 | (OMIM:612286) |
NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 2 | (OMIM:612287) |
Navajo neurohepatopathy | (Orphanet:255229) |
Neonatal severe primary hyperparathyroidism | (Orphanet:417) |
OSTEOGENESIS IMPERFECTA, TYPE VI | (OMIM:613982) |
OSTEOGENESIS IMPERFECTA, TYPE VIII | (OMIM:610915) |
OSTEOGENESIS IMPERFECTA, TYPE XI | (OMIM:610968) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Osteocraniostenosis | (Orphanet:2763) |
Osteogenesis imperfecta | (Orphanet:666) |
Osteogenesis imperfecta - retinopathy - seizures - intellectual deficit | (Orphanet:2773) |
Osteogenesis imperfecta type 1 | (Orphanet:216796) |
Osteoglophonic dwarfism | (Orphanet:2645) |
Osteopenia - myopia - hearing loss - intellectual deficit - facial dysmorphism | (Orphanet:91133) |
Osteopetrosis | (Orphanet:2781) |
Osteopetrosis with renal tubular acidosis | (Orphanet:2785) |
Osteoporosis - pseudoglioma | (Orphanet:2788) |
PAGET DISEASE OF BONE | (OMIM:602080) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Primary hyperoxaluria | (Orphanet:416) |
Primary pigmented nodular adrenocortical disease | (Orphanet:189439) |
Proximal spinal muscular atrophy | (Orphanet:70) |
Pycnodysostosis | (Orphanet:763) |
Pyle disease | (Orphanet:3005) |
SAPHO syndrome | (Orphanet:793) |
Sakati-Nyhan syndrome | (Orphanet:3128) |
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus | (Orphanet:137608) |
Spondylometaphyseal dysplasia, 'corner fracture' type | (Orphanet:93315) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |
Suarez-Stickler syndrome | (Orphanet:166277) |
Systemic mastocytosis | (Orphanet:2467) |
Urban-Rogers-Meyer syndrome | (Orphanet:3409) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
X-linked hypophosphatemia | (Orphanet:89936) |
X-linked lethal multiple pterygium syndrome | (Orphanet:79447) |
Yunis-Varon syndrome | (Orphanet:3472) |