Abnormality of the carpal bones

Symptom Information:

Symptom ID: HPO:0001191
Synonyms:
Abnormal carpal bones [HPO:0001191]
Anomalous carpal bones [HPO:0001191]
Carpal bone anomalies [HPO:0001191]
Carpal anomaly [Orphanet:19720]
Abnormal carpal bones [OMIM:Abnormal carpal bones]
Anomalous carpal bones [OMIM:Anomalous carpal bones]
Carpal bone anomalies [OMIM:Carpal bone anomalies]
Wrist/carpal anomalies [Orphanet:19720]
Abnormal carpal bones (in some patients) [OMIM:Abnormal carpal bones (in some patients)]
Quality:
Cross references:
Orphanet:19720 "Wrist/carpal anomalies" [Orphanet:19720]
OMIM: "Abnormal carpal bones" [OMIM:Abnormal carpal bones]
OMIM: "Anomalous carpal bones" [OMIM:Anomalous carpal bones]
OMIM: "Carpal bone anomalies" [OMIM:Carpal bone anomalies]
OMIM: "Abnormal carpal bones (in some patients)" [OMIM:Abnormal carpal bones (in some patients)]
Is a (Direct Parents):
Orphanet Upper limb segmental anomalies
HPO         Abnormality of the hand
HPO         Abnormality of the wrist
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 upper limb joint(HPO:0009810)
                         Abnormality of the wrist(HPO:0003019)
                            Abnormality of the carpal bones(HPO:0001191)
                      Abnormality of the hand(HPO:0001155)
                         Abnormality of the carpal bones(HPO:0001191)
             Abnormal joint morphology(HPO:0001367)
                Abnormality of upper limb joint(HPO:0009810)
                   Abnormality of the wrist(HPO:0003019)
                      Abnormality of the carpal bones(HPO:0001191)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Brachydactyly - elbow wrist dysplasia (Orphanet:1275)
Holt-Oram syndrome (Orphanet:392)
Juberg-Hayward syndrome (Orphanet:2319)
Leri pleonosteosis (Orphanet:2900)
Léri-Weill dyschondrosteosis (Orphanet:240)
Microcephalic primordial dwarfism, Dauber type (Orphanet:319675)