Shortening of all metacarpals

Symptom Information:

Symptom ID: HPO:0005720
Synonyms:
Short metacarpal [Orphanet:20180]
Metacarpal anomalies/Archibald's sign [Orphanet:20180]
Short metacarpals (1 patient) [OMIM:Short metacarpals (1 patient)]
Short metacarpals (2nd, 3rd, 4th, 5th) [OMIM:Short metacarpals (2nd, 3rd, 4th, 5th)]
Short metacarpals (3rd-5th) [OMIM:Short metacarpals (3rd-5th)]
Short metacarpals (4th-5th) [OMIM:Short metacarpals (4th-5th)]
Short metacarpals (especially 4th and 5th) [OMIM:Short metacarpals (especially 4th and 5th)]
Short metacarpals (especially first metacarpal) [OMIM:Short metacarpals (especially first metacarpal)]
Short metacarpals (homozygote) [OMIM:Short metacarpals (homozygote)]
Quality:
Cross references:
HPO:0010049 "Short metacarpal" [Orphanet:20180]
Orphanet:20180 "Metacarpal anomalies/Archibald's sign" [Orphanet:20180]
OMIM: "Short metacarpals (1 patient)" [OMIM:Short metacarpals (1 patient)]
OMIM: "Short metacarpals (2nd, 3rd, 4th, 5th)" [OMIM:Short metacarpals (2nd, 3rd, 4th, 5th)]
OMIM: "Short metacarpals (3rd-5th)" [OMIM:Short metacarpals (3rd-5th)]
OMIM: "Short metacarpals (4th-5th)" [OMIM:Short metacarpals (4th-5th)]
OMIM: "Short metacarpals (especially 4th and 5th)" [OMIM:Short metacarpals (especially 4th and 5th)]
OMIM: "Short metacarpals (especially first metacarpal)" [OMIM:Short metacarpals (especially first metacarpal)]
OMIM: "Short metacarpals (homozygote)" [OMIM:Short metacarpals (homozygote)]
Is a (Direct Parents):
HPO         Short metacarpal
Orphanet Abnormality of the hand
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)
             Aplasia/hypoplasia involving the skeleton(HPO:0009115)
                Aplasia/hypoplasia of the extremities(HPO:0009815)
                   Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                      Aplasia/hypoplasia involving bones of the hand(HPO:0005927)
                         Aplasia/Hypoplasia involving the metacarpal bones(HPO:0005914)
                            Short metacarpal(HPO:0010049)
                               Shortening of all metacarpals(HPO:0005720)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the upper limb(HPO:0002817)
                      Abnormality of the hand(HPO:0001155)
                         Aplasia/hypoplasia involving bones of the hand(HPO:0005927)
                            Aplasia/Hypoplasia involving the metacarpal bones(HPO:0005914)
                               Short metacarpal(HPO:0010049)
                                  Shortening of all metacarpals(HPO:0005720)
                         Abnormality of the metacarpal bones(HPO:0001163)
                            Abnormal metacarpal morphology(HPO:0005916)
                               Aplasia/Hypoplasia involving the metacarpal bones(HPO:0005914)
                                  Short metacarpal(HPO:0010049)
                                     Shortening of all metacarpals(HPO:0005720)
                      Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                         Aplasia/hypoplasia involving bones of the hand(HPO:0005927)
                            Aplasia/Hypoplasia involving the metacarpal bones(HPO:0005914)
                               Short metacarpal(HPO:0010049)
                                  Shortening of all metacarpals(HPO:0005720)
                   Aplasia/hypoplasia of the extremities(HPO:0009815)
                      Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                         Aplasia/hypoplasia involving bones of the hand(HPO:0005927)
                            Aplasia/Hypoplasia involving the metacarpal bones(HPO:0005914)
                               Short metacarpal(HPO:0010049)
                                  Shortening of all metacarpals(HPO:0005720)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Acro-oto-ocular syndrome (Orphanet:2980)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Czech dysplasia, metatarsal type (Orphanet:137678)
Fibular aplasia - complex brachydactyly (Orphanet:2639)
LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE (OMIM:601356)
Oculoosteocutaneous syndrome (Orphanet:2713)
PELGER-HUET ANOMALY (OMIM:169400)
Pseudohypoparathyroidism type 1A (Orphanet:79443)
Pseudohypoparathyroidism type 1C (Orphanet:79444)
Pseudopseudohypoparathyroidism (Orphanet:79445)
SATOYOSHI SYNDROME (OMIM:600705)
Spondyloperipheral dysplasia - short ulna (Orphanet:1856)