Aplasia/Hypoplasia of the middle phalanges of the hand
Symptom Information:
Symptom ID: | HPO:0009843 | |||||||||||||||
Synonyms: |
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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 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) 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) MedDRA: |
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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) |