Aplasia/Hypoplasia of the phalanges of the hand

Symptom Information:

Symptom ID: HPO:0009767
Synonyms:
Aplastic/hypoplastic phalanges [HPO:0009767]
Aplastic/hypoplastic phalanges of the hand [HPO:0009767]
Hypoplastic/absent phalanges [HPO:0009767]
Aplastic/hypoplastic phalanges [OMIM:Aplastic/hypoplastic phalanges]
Hypoplastic/absent phalanges [OMIM:Hypoplastic/absent phalanges]
Quality:
Cross references:
OMIM: "Aplastic/hypoplastic phalanges" [OMIM:Aplastic/hypoplastic phalanges]
OMIM: "Hypoplastic/absent phalanges" [OMIM:Hypoplastic/absent phalanges]
Is a (Direct Parents):
HPO         Abnormality of phalanx of finger
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)
                   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)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive Robinow syndrome (Orphanet:1507)
Fraser syndrome (Orphanet:2052)
Fuhrmann syndrome (Orphanet:2854)
Phocomelia, Schinzel type (Orphanet:2879)
SPLIT-HAND/FOOT MALFORMATION 4 (OMIM:605289)