Brachytelomesophalangy

Symptom Information:

Symptom ID: HPO:0005872
Synonyms:
Progressive brachydactyly of middle and distal phalanges [HPO:0005872]
Short middle and distal phalanges of digits ii through v [HPO:0005872]
Brachytelomesophalangy [OMIM:Brachytelomesophalangy]
Progressive brachydactyly of middle and distal phalanges [OMIM:Progressive brachydactyly of middle and distal phalanges]
Short middle and distal phalanges of digits II through V [OMIM:Short middle and distal phalanges of digits II through V]
Quality:
Cross references:
OMIM: "Brachytelomesophalangy" [OMIM:Brachytelomesophalangy]
OMIM: "Progressive brachydactyly of middle and distal phalanges" [OMIM:Progressive brachydactyly of middle and distal phalanges]
OMIM: "Short middle and distal phalanges of digits II through V" [OMIM:Short middle and distal phalanges of digits II through V]
Is a (Direct Parents):
HPO         Brachydactyly syndrome
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)
                         Brachydactyly syndrome(HPO:0001156)
                            Brachytelomesophalangy(HPO:0005872)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Cryptomicrotia - brachydactyly - excess fingertip arch (Orphanet:1547)
Familial digital arthropathy-brachydactyly (Orphanet:85169)