Delayed ossification of carpal bones

Symptom Information:

Symptom ID: HPO:0001216
Synonyms:
Carpal delayed ossification [HPO:0001216]
Delayed carpal bone age [HPO:0001216]
Delayed carpal ossification [HPO:0001216]
Delayed maturation of carpal bones [HPO:0001216]
Delayed bone age [Orphanet:45360]
Delayed bone age (finding) [Orphanet:45360]
Carpal delayed ossification [OMIM:Carpal delayed ossification]
Delayed carpal bone age [OMIM:Delayed carpal bone age]
Delayed carpal ossification [OMIM:Delayed carpal ossification]
Age bone retarded [Orphanet:45360]
Epiphyses delayed fusion [MedDRA:10015077]
Age bone retarded [MedDRA:10015077]
Closure delayed epiphysis [MedDRA:10015077]
Epiphysis closure delayed [MedDRA:10015077]
Bone age delay [OMIM:Bone age delay]
Carpal ossification delay [OMIM:Carpal ossification delay]
Delayed bone age (in 1/4 patients) [OMIM:Delayed bone age (in 1/4 patients)]
Delayed bone age (in male and female patients) [OMIM:Delayed bone age (in male and female patients)]
Delayed bone age (in some patients) [OMIM:Delayed bone age (in some patients)]
Quality:
Cross references:
HPO:0002750 "Delayed skeletal maturation" [Orphanet:45360]
Orphanet:45360 "Delayed bone age" [Orphanet:45360]
OMIM: "Carpal delayed ossification" [OMIM:Carpal delayed ossification]
OMIM: "Delayed carpal bone age" [OMIM:Delayed carpal bone age]
OMIM: "Delayed carpal ossification" [OMIM:Delayed carpal ossification]
OMIM: "Bone age delay" [OMIM:Bone age delay]
OMIM: "Carpal ossification delay" [OMIM:Carpal ossification delay]
OMIM: "Delayed bone age (in 1/4 patients)" [OMIM:Delayed bone age (in 1/4 patients)]
OMIM: "Delayed bone age (in male and female patients)" [OMIM:Delayed bone age (in male and female patients)]
OMIM: "Delayed bone age (in some patients)" [OMIM:Delayed bone age (in some patients)]
UMLS:C0541764 "Delayed bone age" [Orphanet:45360]
Is a (Direct Parents):
MedDRA Epiphyseal disorders
Orphanet Abnormality of the skeletal system
HPO         Abnormality of carpal bone ossification
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 bone structure(HPO:0003330)
                Abnormal bone ossification(HPO:0011849)
                   Abnormal hand bone ossification(HPO:0010660)
                      Abnormality of carpal bone ossification(HPO:0006257)
                         Delayed ossification of carpal bones(HPO:0001216)
             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 carpal bone ossification(HPO:0006257)
                                  Delayed ossification of carpal bones(HPO:0001216)
                      Abnormality of the hand(HPO:0001155)
                         Abnormal hand bone ossification(HPO:0010660)
                            Abnormality of carpal bone ossification(HPO:0006257)
                               Delayed ossification of carpal bones(HPO:0001216)
                         Abnormality of the carpal bones(HPO:0001191)
                            Abnormality of carpal bone ossification(HPO:0006257)
                               Delayed ossification of carpal bones(HPO:0001216)
             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)
                         Abnormality of carpal bone ossification(HPO:0006257)
                            Delayed ossification of carpal bones(HPO:0001216)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Bone disorders (excl congenital and fractures)(MedDRA:10005959)
       Epiphyseal disorders(MedDRA:10015072)
          Delayed ossification of carpal bones(HPO:0001216)
Database Frequency: 30 / 7739
Resource:

All diseases associated with this symptom:

Acrocapitofemoral dysplasia (Orphanet:63446)
Anauxetic dysplasia (Orphanet:93347)
Angel-shaped phalango-epiphyseal dysplasia (Orphanet:63442)
Bloom syndrome (Orphanet:125)
CODAS syndrome (Orphanet:1458)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Cystinosis (Orphanet:213)
DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES (OMIM:127200)
ESTROGEN RESISTANCE (OMIM:615363)
Gaucher disease (Orphanet:355)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 3 (Orphanet:77261)
Goldblatt syndrome (Orphanet:166272)
Hand-foot-genital syndrome (Orphanet:2438)
Hurler syndrome (Orphanet:93473)
Hyperphosphatasia-intellectual deficiency syndrome (Orphanet:247262)
Kearns-Sayre syndrome (Orphanet:480)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
Leprechaunism (Orphanet:508)
MELAS (Orphanet:550)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2 (OMIM:614114)
Multiple epiphyseal dysplasia type 5 (Orphanet:93311)
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY (OMIM:614800)
SKELETAL DYSPLASIA WITH DELAYED EPIPHYSEAL AND CARPAL BONE OSSIFICATION (OMIM:182255)
SPONASTRIME dysplasia (Orphanet:93357)
SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS (OMIM:609616)
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome (Orphanet:314394)
Wiedemann-Steiner syndrome (Orphanet:319182)
Wolcott-Rallison syndrome (Orphanet:1667)