Hand monodactyly

Symptom Information:

Symptom ID: HPO:0004058
Synonyms:
Monodactyly [OMIM:Monodactyly]
Monodactyly (some) [OMIM:Monodactyly (some)]
Quality:
Cross references:
OMIM: "Monodactyly" [OMIM:Monodactyly]
OMIM: "Monodactyly (some)" [OMIM:Monodactyly (some)]
Is a (Direct Parents):
HPO         Hand oligodactyly
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)
                      Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                         Aplasia/hypoplasia involving bones of the hand(HPO:0005927)
                            Aplasia/Hypoplasia of fingers(HPO:0006265)
                               Aplasia of the fingers(HPO:0009380)
                                  Hand oligodactyly(HPO:0001180)
                                     Hand monodactyly(HPO:0004058)
                      Abnormality of the hand(HPO:0001155)
                         Abnormality of finger(HPO:0001167)
                            Aplasia/Hypoplasia of fingers(HPO:0006265)
                               Aplasia of the fingers(HPO:0009380)
                                  Hand oligodactyly(HPO:0001180)
                                     Hand monodactyly(HPO:0004058)
                         Aplasia/hypoplasia involving bones of the hand(HPO:0005927)
                            Aplasia/Hypoplasia of fingers(HPO:0006265)
                               Aplasia of the fingers(HPO:0009380)
                                  Hand oligodactyly(HPO:0001180)
                                     Hand monodactyly(HPO:0004058)
                   Abnormality of digit(HPO:0011297)
                      Oligodactyly(HPO:0012165)
                         Hand oligodactyly(HPO:0001180)
                            Hand monodactyly(HPO:0004058)
                      Abnormality of finger(HPO:0001167)
                         Aplasia/Hypoplasia of fingers(HPO:0006265)
                            Aplasia of the fingers(HPO:0009380)
                               Hand oligodactyly(HPO:0001180)
                                  Hand monodactyly(HPO:0004058)
                   Aplasia/hypoplasia of the extremities(HPO:0009815)
                      Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                         Aplasia/hypoplasia involving bones of the hand(HPO:0005927)
                            Aplasia/Hypoplasia of fingers(HPO:0006265)
                               Aplasia of the fingers(HPO:0009380)
                                  Hand oligodactyly(HPO:0001180)
                                     Hand monodactyly(HPO:0004058)
             Aplasia/hypoplasia involving the skeleton(HPO:0009115)
                Aplasia/hypoplasia of the extremities(HPO:0009815)
                   Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                      Aplasia/hypoplasia involving bones of the hand(HPO:0005927)
                         Aplasia/Hypoplasia of fingers(HPO:0006265)
                            Aplasia of the fingers(HPO:0009380)
                               Hand oligodactyly(HPO:0001180)
                                  Hand monodactyly(HPO:0004058)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
CHARGE syndrome (Orphanet:138)
CHROMOSOME 17p13.3, TELOMERIC, DUPLICATION SYNDROME (OMIM:612576)
Gollop-Wolfgang complex (Orphanet:1986)
Karsch-Neugebauer syndrome (Orphanet:2329)
SPLIT-HAND/FOOT MALFORMATION 1 (OMIM:183600)
Tetramelic monodactyly (Orphanet:2564)
Tibial aplasia - ectrodactyly (Orphanet:3329)