Long fingers

Symptom Information:

Symptom ID: HPO:0100807
Synonyms:
Long fingers [OMIM:Long fingers]
Long hand/arachnodactyly [Orphanet:20120]
Long fingers (2 patient) [OMIM:Long fingers (2 patient)]
Long fingers (rare) [OMIM:Long fingers (rare)]
Quality:
Cross references:
HPO:0001166 "Arachnodactyly" [Orphanet:20120]
Orphanet:20120 "Long hand/arachnodactyly" [Orphanet:20120]
OMIM: "Long fingers" [OMIM:Long fingers]
OMIM: "Long fingers (2 patient)" [OMIM:Long fingers (2 patient)]
OMIM: "Long fingers (rare)" [OMIM:Long fingers (rare)]
Is a (Direct Parents):
HPO         Abnormality of finger
Orphanet Abnormality of the hand
Orphanet Arachnodactyly
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)
                            Long fingers(HPO:0100807)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of finger(HPO:0001167)
                         Long fingers(HPO:0100807)
MedDRA:
Database Frequency: 23 / 7739
Resource:

All diseases associated with this symptom:

16p13.3 microduplication syndrome (Orphanet:96078)
17q12 microdeletion syndrome (Orphanet:261265)
17q23.1q23.2 microdeletion syndrome (Orphanet:261279)
5p13 microduplication syndrome (Orphanet:329802)
ALG3-CDG (Orphanet:79321)
Acute infantile liver failure-multisystemic involvement syndrome (Orphanet:370088)
Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet:1154)
CANDLE syndrome (Orphanet:325004)
CHROMOSOME 15q25 DELETION SYNDROME (OMIM:614294)
CHROMOSOME 5q12 DELETION SYNDROME (OMIM:615668)
Craniofacial dysplasia-osteopenia syndrome (Orphanet:314555)
EPIPHYSEAL DYSPLASIA, BAUMANN TYPE (OMIM:610797)
Intellectual deficit, X-linked, Snyder type (Orphanet:3063)
JMP syndrome (Orphanet:324999)
KAGAMI-OGATA SYNDROME (OMIM:608149)
LUJAN-FRYNS SYNDROME (OMIM:309520)
MENTAL RETARDATION, X-LINKED, SYNDROMIC 14 (OMIM:300676)
Nakajo-Nishimura syndrome (Orphanet:2615)
PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES (OMIM:602249)
Proteasome disability syndrome (Orphanet:324977)
Spondylo-ocular syndrome (Orphanet:85194)
Stickler syndrome type 2 (Orphanet:90654)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)