Aplasia/Hypoplasia of the middle phalanges of the hand

Symptom Information:

Symptom ID: HPO:0009843
Synonyms:
Absent/hypoplastic middle phalanges [HPO:0009843]
Aplasia/hypoplasia of middle phalanges [HPO:0009843]
Aplastic/hypoplastic middle phalanges [HPO:0009843]
Hypoplastic/aplastic middle phalanx [HPO:0009843]
Short to absent middle phalanges [HPO:0009843]
Short/absent middle phalanges [HPO:0009843]
Absent/hypoplastic middle phalanges [OMIM:Absent/hypoplastic middle phalanges]
Aplasia/hypoplasia of middle phalanges [OMIM:Aplasia/hypoplasia of middle phalanges]
Aplastic/hypoplastic middle phalanges [OMIM:Aplastic/hypoplastic middle phalanges]
Hypoplastic/aplastic middle phalanx [OMIM:Hypoplastic/aplastic middle phalanx]
Short to absent middle phalanges [OMIM:Short to absent middle phalanges]
Short/absent middle phalanges [OMIM:Short/absent middle phalanges]
Aplastic/hypoplastic middle phalanges (fingers 2-5) [OMIM:Aplastic/hypoplastic middle phalanges (fingers 2-5)]
Aplastic/hypoplastic middle phalanges (toes 2-5) [OMIM:Aplastic/hypoplastic middle phalanges (toes 2-5)]
Hypoplastic/aplastic middle phalanx (2nd finger) [OMIM:Hypoplastic/aplastic middle phalanx (2nd finger)]
Quality:
Cross references:
OMIM: "Absent/hypoplastic middle phalanges" [OMIM:Absent/hypoplastic middle phalanges]
OMIM: "Aplasia/hypoplasia of middle phalanges" [OMIM:Aplasia/hypoplasia of middle phalanges]
OMIM: "Aplastic/hypoplastic middle phalanges" [OMIM:Aplastic/hypoplastic middle phalanges]
OMIM: "Hypoplastic/aplastic middle phalanx" [OMIM:Hypoplastic/aplastic middle phalanx]
OMIM: "Short to absent middle phalanges" [OMIM:Short to absent middle phalanges]
OMIM: "Short/absent middle phalanges" [OMIM:Short/absent middle phalanges]
OMIM: "Aplastic/hypoplastic middle phalanges (fingers 2-5)" [OMIM:Aplastic/hypoplastic middle phalanges (fingers 2-5)]
OMIM: "Aplastic/hypoplastic middle phalanges (toes 2-5)" [OMIM:Aplastic/hypoplastic middle phalanges (toes 2-5)]
OMIM: "Hypoplastic/aplastic middle phalanx (2nd finger)" [OMIM:Hypoplastic/aplastic middle phalanx (2nd finger)]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of the phalanges of the hand
HPO         Abnormality of the middle phalanges 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 the upper limb(HPO:0002817)
                      Abnormality of the hand(HPO:0001155)
                         Abnormality of finger(HPO:0001167)
                            Abnormality of phalanx of finger(HPO:0005918)
                               Aplasia/Hypoplasia of the phalanges of the hand(HPO:0009767)
                                  Aplasia/Hypoplasia of the middle phalanges of the hand(HPO:0009843)
                               Abnormality of the middle phalanges of the hand(HPO:0009833)
                                  Aplasia/Hypoplasia of the middle phalanges of the hand(HPO:0009843)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of finger(HPO:0001167)
                         Abnormality of phalanx of finger(HPO:0005918)
                            Aplasia/Hypoplasia of the phalanges of the hand(HPO:0009767)
                               Aplasia/Hypoplasia of the middle phalanges of the hand(HPO:0009843)
                            Abnormality of the middle phalanges of the hand(HPO:0009833)
                               Aplasia/Hypoplasia of the middle phalanges of the hand(HPO:0009843)
MedDRA:
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

BRACHYDACTYLY, TYPE A1 (OMIM:112500)
Brachydactyly type A2 (Orphanet:93396)
Brachydactyly type A6 (Orphanet:93382)
Brachydactyly type B2 (Orphanet:140908)
Carpenter syndrome (Orphanet:65759)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
MULTIPLE SYNOSTOSES SYNDROME 1 (OMIM:186500)
Multiple synostoses syndrome (Orphanet:3237)
Proximal symphalangism (Orphanet:3250)
SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH (OMIM:606895)
SYNOSTOSES, TARSAL, CARPAL, AND DIGITAL (OMIM:186400)
Tarsal-carpal coalition syndrome (Orphanet:1412)
Yunis-Varon syndrome (Orphanet:3472)