Delayed ossification of carpal bones
Symptom Information:
Symptom ID: | HPO:0001216 | |||||||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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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 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) 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) Abnormality of the carpal bones(HPO:0001191) Abnormality of carpal bone ossification(HPO:0006257) Delayed ossification of carpal bones(HPO:0001216) Abnormal hand bone ossification(HPO:0010660) 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) |
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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) |