Aplasia/Hypoplasia of the distal phalanges of the hand
Symptom Information:
Symptom ID: | HPO:0009835 | |||||||||||||||||
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 the upper limb(HPO:0002817) Abnormality of the hand(HPO:0001155) Abnormality of finger(HPO:0001167) Abnormality of phalanx of finger(HPO:0005918) Abnormality of the distal phalanx of finger(HPO:0009832) Aplasia/Hypoplasia of the distal phalanges of the hand(HPO:0009835) Aplasia/Hypoplasia of the phalanges of the hand(HPO:0009767) Aplasia/Hypoplasia of the distal phalanges of the hand(HPO:0009835) Abnormality of digit(HPO:0011297) Abnormality of finger(HPO:0001167) Abnormality of phalanx of finger(HPO:0005918) Abnormality of the distal phalanx of finger(HPO:0009832) Aplasia/Hypoplasia of the distal phalanges of the hand(HPO:0009835) Aplasia/Hypoplasia of the phalanges of the hand(HPO:0009767) Aplasia/Hypoplasia of the distal phalanges of the hand(HPO:0009835) MedDRA: |
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Database Frequency: | 9 / 7739 | |||||||||||||||||
Resource: |
All diseases associated with this symptom:
ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY | (OMIM:106990) |
Autosomal recessive deafness-onychodystrophy syndrome | (Orphanet:79500) |
Brachydactyly type B | (Orphanet:93383) |
Brachydactyly type B2 | (Orphanet:140908) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
MULTIPLE SYNOSTOSES SYNDROME 1 | (OMIM:186500) |
Microcephaly-capillary malformation syndrome | (Orphanet:294016) |
SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH | (OMIM:606895) |
Yunis-Varon syndrome | (Orphanet:3472) |