Hand oligodactyly

Symptom Information:

Symptom ID: HPO:0001180
Synonyms:
Absent finger [Orphanet:20540]
Absent finger (disorder) [Orphanet:20540]
Oligodactyly/ectrodactyly of fingers [Orphanet:20540]
Oligodactyly [Orphanet:20540]
Adactyly [MedDRA:10049207]
Oligodactyly [MedDRA:10049207]
Oligodactyly (45%) [OMIM:Oligodactyly (45%)]
Quality:
Cross references:
HPO:0001171 "Ectrodactyly (hands)" [Orphanet:20540]
HPO:0009380 "Aplasia of the fingers" [Orphanet:20540]
Orphanet:20540 "Oligodactyly/ectrodactyly of fingers" [Orphanet:20540]
OMIM: "Oligodactyly (45%)" [OMIM:Oligodactyly (45%)]
UMLS:C0728895 "Absent finger" [Orphanet:20540]
Is a (Direct Parents):
Orphanet Abnormality of the hand
HPO         Oligodactyly
MedDRA Musculoskeletal and connective tissue disorders of limbs congenital
HPO         Aplasia of the fingers
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)
             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)
             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)
                      Abnormality of the hand(HPO:0001155)
                         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)
                         Abnormality of finger(HPO:0001167)
                            Aplasia/Hypoplasia of fingers(HPO:0006265)
                               Aplasia of the fingers(HPO:0009380)
                                  Hand oligodactyly(HPO:0001180)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of finger(HPO:0001167)
                         Aplasia/Hypoplasia of fingers(HPO:0006265)
                            Aplasia of the fingers(HPO:0009380)
                               Hand oligodactyly(HPO:0001180)
                      Oligodactyly(HPO:0012165)
                         Hand oligodactyly(HPO:0001180)
                   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)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396)
       Musculoskeletal and connective tissue disorders of limbs congenital(MedDRA:10028381)
          Hand oligodactyly(HPO:0001180)
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

Acrorenal syndrome (Orphanet:971)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Cornelia de Lange syndrome (Orphanet:199)
FIBULAR APLASIA, TIBIAL CAMPOMELIA, AND OLIGOSYNDACTYLY SYNDROME (OMIM:246570)
Focal dermal hypoplasia (Orphanet:2092)
Fuhrmann syndrome (Orphanet:2854)
Microgastria - limb reduction defect (Orphanet:2538)
Microphthalmia with limb anomalies (Orphanet:1106)
Orofaciodigital syndrome type 10 (Orphanet:2756)
Phocomelia, Schinzel type (Orphanet:2879)
Roberts syndrome (Orphanet:3103)
Robin sequence - oligodactyly (Orphanet:3104)
SPLIT-HAND/FOOT MALFORMATION 6 (OMIM:225300)
Split hand-split foot malformation (Orphanet:2440)
ULNAR AGENESIS AND ENDOCARDIAL FIBROELASTOSIS (OMIM:276822)
WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME (OMIM:602418)
XK aprosencephaly (Orphanet:3469)