Hyperextensibility of the finger joints

Symptom Information:

Symptom ID: HPO:0001187
Synonyms:
Hyperextensible digits [HPO:0001187]
Hyperextensible finger [HPO:0001187]
Hyperextensible fingers [HPO:0001187]
Hyperextensible digits [OMIM:Hyperextensible digits]
Hyperextensible finger [OMIM:Hyperextensible finger]
Hyperextensible fingers [OMIM:Hyperextensible fingers]
Quality:
Cross references:
OMIM: "Hyperextensible digits" [OMIM:Hyperextensible digits]
OMIM: "Hyperextensible finger" [OMIM:Hyperextensible finger]
OMIM: "Hyperextensible fingers" [OMIM:Hyperextensible fingers]
Is a (Direct Parents):
HPO         Joint hypermobility
HPO         Abnormality of finger
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 upper limb(HPO:0002817)
                      Abnormality of the hand(HPO:0001155)
                         Abnormality of finger(HPO:0001167)
                            Hyperextensibility of the finger joints(HPO:0001187)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of finger(HPO:0001167)
                         Hyperextensibility of the finger joints(HPO:0001187)
             Abnormal joint morphology(HPO:0001367)
                Abnormality of joint mobility(HPO:0011729)
                   Joint hypermobility(HPO:0001382)
                      Hyperextensibility of the finger joints(HPO:0001187)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

AARSKOG-SCOTT SYNDROME (OMIM:305400)
Angel-shaped phalango-epiphyseal dysplasia (Orphanet:63442)
CARDIOFACIOCUTANEOUS SYNDROME 1 (OMIM:115150)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Coffin-Lowry syndrome (Orphanet:192)
Costello syndrome (Orphanet:3071)
Geroderma osteodysplastica (Orphanet:2078)
Intellectual deficit, X-linked, Snyder type (Orphanet:3063)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
MARFANOID HABITUS WITH SITUS INVERSUS (OMIM:609008)
Spondylometaphyseal dysplasia, Golden type (Orphanet:168544)
Zimmermann-Laband syndrome (Orphanet:3473)