Short metatarsal

Symptom Information:

Symptom ID: HPO:0010743
Synonyms:
Hypoplasia of the metatarsal bones [HPO:0010743]
Hypoplastic metatarsals [HPO:0010743]
Short metatarsal bone [HPO:0010743]
SHORT METATARSAL BONES [HPO:0010743]
Short metatarsals [HPO:0010743]
Shortened metatarsals [HPO:0010743]
Hypoplastic metatarsals [OMIM:Hypoplastic metatarsals]
Short metatarsal [OMIM:Short metatarsal]
Short metatarsal bones [OMIM:Short metatarsal bones]
Short metatarsals [OMIM:Short metatarsals]
Shortened metatarsals [OMIM:Shortened metatarsals]
Malimplantation of toes [Orphanet:22360]
Hypoplastic metatarsals (3rd and 4th) [OMIM:Hypoplastic metatarsals (3rd and 4th)]
Short metatarsals (1 patient) [OMIM:Short metatarsals (1 patient)]
Short metatarsals (4th) [OMIM:Short metatarsals (4th)]
Short metatarsals (4th-5th) [OMIM:Short metatarsals (4th-5th)]
Short metatarsals (especially 4th and 5th) [OMIM:Short metatarsals (especially 4th and 5th)]
Short metatarsals (especially first metatarsal) [OMIM:Short metatarsals (especially first metatarsal)]
Quality:
Cross references:
HPO:0004686 "Short third metatarsal" [Orphanet:22360]
Orphanet:22360 "Malimplantation of toes" [Orphanet:22360]
OMIM: "Hypoplastic metatarsals" [OMIM:Hypoplastic metatarsals]
OMIM: "Short metatarsal" [OMIM:Short metatarsal]
OMIM: "Short metatarsal bones" [OMIM:Short metatarsal bones]
OMIM: "Short metatarsals" [OMIM:Short metatarsals]
OMIM: "Shortened metatarsals" [OMIM:Shortened metatarsals]
OMIM: "Hypoplastic metatarsals (3rd and 4th)" [OMIM:Hypoplastic metatarsals (3rd and 4th)]
OMIM: "Short metatarsals (1 patient)" [OMIM:Short metatarsals (1 patient)]
OMIM: "Short metatarsals (4th)" [OMIM:Short metatarsals (4th)]
OMIM: "Short metatarsals (4th-5th)" [OMIM:Short metatarsals (4th-5th)]
OMIM: "Short metatarsals (especially 4th and 5th)" [OMIM:Short metatarsals (especially 4th and 5th)]
OMIM: "Short metatarsals (especially first metatarsal)" [OMIM:Short metatarsals (especially first metatarsal)]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of metatarsal bones
Orphanet Abnormality of the foot
HPO         Short long bone
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)
                   Abnormality of the lower limb(HPO:0002814)
                      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 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)
                   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)
             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)
MedDRA:
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)