Short digit

Symptom Information:

Symptom ID: HPO:0011927
Synonyms:
VERY SHORT DIGITS [HPO:0011927]
Short finger [Orphanet:20060]
Brachydactyly of hand (disorder) [Orphanet:20060]
Short finger (finding) [Orphanet:20060]
Brachydactyly of hand [Orphanet:20060]
Very short digits [OMIM:Very short digits]
Short hand/brachydactyly [Orphanet:20060]
Short digits [OMIM:Short digits]
Quality:
Cross references:
HPO:0009381 "Short finger" [Orphanet:20060]
HPO:0009803 "Short phalanx of finger" [Orphanet:20060]
Orphanet:20060 "Short hand/brachydactyly" [Orphanet:20060]
OMIM: "Very short digits" [OMIM:Very short digits]
OMIM: "Short digits" [OMIM:Short digits]
UMLS:C0588368 "Brachydactyly of hand" [Orphanet:20060]
UMLS:C0239594 "Short finger" [Orphanet:20060]
Is a (Direct Parents):
HPO         Abnormality of digit
Orphanet Short palm
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)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of digit(HPO:0011297)
                      Short digit(HPO:0011927)
MedDRA:
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

AREDYLD syndrome (Orphanet:1133)
Acromesomelic dysplasia, Grebe type (Orphanet:2098)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 12 (OMIM:615989)
Bardet-Biedl syndrome 18 (OMIM:615995)
Bardet-Biedl syndrome 2 (OMIM:615981)
Bardet-Biedl syndrome 4 (OMIM:615982)
Bardet-Biedl syndrome 7 (OMIM:615984)
Bardet-Biedl syndrome 9 (OMIM:615986)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Microcephalic osteodysplastic dysplasia, Saul-Wilson type (Orphanet:85172)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Rabson-Mendenhall syndrome (Orphanet:769)
Rudiger syndrome (Orphanet:3118)
SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES (OMIM:615789)
Wolcott-Rallison syndrome (Orphanet:1667)