Long fingers
Symptom Information:
Symptom ID: | HPO:0100807 | ||||||
Synonyms: |
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Quality: | |||||||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |