Short metatarsal
Symptom Information:
Symptom ID: | HPO:0010743 | ||||||||||||||||||
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 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 lower limbs(HPO:0006493) Aplasia/Hypoplasia involving bones of the feet(HPO:0006494) Aplasia/Hypoplasia of metatarsal bones(HPO:0001964) Short metatarsal(HPO:0010743) Abnormality of the lower limb(HPO:0002814) Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493) Aplasia/Hypoplasia involving bones of the feet(HPO:0006494) Aplasia/Hypoplasia of metatarsal bones(HPO:0001964) Short metatarsal(HPO:0010743) Abnormality of the foot(HPO:0001760) Abnormality of the metatarsal bones(HPO:0001832) Aplasia/Hypoplasia of metatarsal bones(HPO:0001964) Short metatarsal(HPO:0010743) Aplasia/Hypoplasia involving bones of the feet(HPO:0006494) Aplasia/Hypoplasia of metatarsal bones(HPO:0001964) Short metatarsal(HPO:0010743) Aplasia/hypoplasia involving the skeleton(HPO:0009115) Aplasia/hypoplasia of the extremities(HPO:0009815) Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493) Aplasia/Hypoplasia involving bones of the feet(HPO:0006494) Aplasia/Hypoplasia of metatarsal bones(HPO:0001964) Short metatarsal(HPO:0010743) Abnormality of long bone morphology(HPO:0011314) Short long bone(HPO:0003026) Short metatarsal(HPO:0010743) MedDRA: |
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Database Frequency: | 56 / 7739 | ||||||||||||||||||
Resource: |
All diseases associated with this symptom:
19q13.11 microdeletion syndrome | (Orphanet:217346) |
2q37 microdeletion syndrome | (Orphanet:1001) |
ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE | (OMIM:101800) |
ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE | (OMIM:614613) |
ADAMS-OLIVER SYNDROME 3 | (OMIM:614814) |
ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY | (OMIM:106990) |
Acrodysostosis with multiple hormone resistance | (Orphanet:280651) |
Acromesomelic dysplasia, Maroteaux type | (Orphanet:40) |
Albright hereditary osteodystrophy | (Orphanet:665) |
Atelosteogenesis type I | (Orphanet:1190) |
Autosomal dominant Larsen syndrome | (Orphanet:503) |
BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION | (OMIM:613627) |
BRACHYDACTYLY, TYPE E, WITH ATRIAL SEPTAL DEFECT, TYPE II | (OMIM:113301) |
BRACHYDACTYLY, TYPE E2 | (OMIM:613382) |
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA | (OMIM:609945) |
Brachydactyly - nystagmus - cerebellar ataxia | (Orphanet:1246) |
Brachydactyly - preaxial hallux varus | (Orphanet:1278) |
Brachydactyly type E | (Orphanet:93387) |
Camptodactyly syndrome, Guadalajara type 1 | (Orphanet:1327) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Cohen syndrome | (Orphanet:193) |
Combined immunodeficiency with facio-oculo-skeletal anomalies | (Orphanet:221139) |
Czech dysplasia, metatarsal type | (Orphanet:137678) |
DESBUQUOIS DYSPLASIA 1 | (OMIM:251450) |
DYGGVE-MELCHIOR-CLAUSEN DISEASE | (OMIM:223800) |
Desbuquois syndrome | (Orphanet:1425) |
Dyggve-Melchior-Clausen disease | (Orphanet:239) |
Fibular aplasia - complex brachydactyly | (Orphanet:2639) |
Focal dermal hypoplasia | (Orphanet:2092) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
Jackson-Weiss syndrome | (Orphanet:1540) |
Leri pleonosteosis | (Orphanet:2900) |
Marinesco-Sjögren syndrome | (Orphanet:559) |
Metaphyseal chondrodysplasia, Kaitila type | (Orphanet:166038) |
Monosomy 5p | (Orphanet:281) |
Oculoosteocutaneous syndrome | (Orphanet:2713) |
Osteoglophonic dwarfism | (Orphanet:2645) |
Otopalatodigital syndrome | (Orphanet:669) |
Otopalatodigital syndrome type 2 | (Orphanet:90652) |
Paraplegia - brachydactyly - cone-shaped epiphysis | (Orphanet:2823) |
Peters-plus syndrome | (Orphanet:709) |
Pseudohypoparathyroidism type 1A | (Orphanet:79443) |
Pseudohypoparathyroidism type 1C | (Orphanet:79444) |
Pseudopseudohypoparathyroidism | (Orphanet:79445) |
Ruvalcaba syndrome | (Orphanet:3121) |
SATOYOSHI SYNDROME | (OMIM:600705) |
SMITH-MCCORT DYSPLASIA 2 | (OMIM:615222) |
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome | (Orphanet:314394) |
Spondyloepimetaphyseal dysplasia, Irapa type | (Orphanet:93351) |
Spondyloperipheral dysplasia - short ulna | (Orphanet:1856) |
TRICHORHINOPHALANGEAL SYNDROME, TYPE I | (OMIM:190350) |
TRICHORHINOPHALANGEAL SYNDROME, TYPE III | (OMIM:190351) |
Temtamy preaxial brachydactyly syndrome | (Orphanet:363417) |
Townes-Brocks syndrome | (Orphanet:857) |
Trichorhinophalangeal syndrome type 1 and 3 | (Orphanet:77258) |
Zechi-Ceide syndrome | (Orphanet:217017) |