11 pairs of ribs

Symptom Information:

Symptom ID: HPO:0000878
Synonyms:
11 pairs of ribs [OMIM:11 pairs of ribs]
Quality:
Cross references:
OMIM: "11 pairs of ribs" [OMIM:11 pairs of ribs]
Is a (Direct Parents):
HPO         Missing ribs
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 affecting bones of the axial skeleton(HPO:0009122)
                   Aplasia/Hypoplasia involving bones of the thorax(HPO:0006711)
                      Aplasia/Hypoplasia of the ribs(HPO:0006712)
                         Missing ribs(HPO:0000921)
                            11 pairs of ribs(HPO:0000878)
             Abnormal axial skeleton morphology(HPO:0009121)
                Aplasia/hypoplasia affecting bones of the axial skeleton(HPO:0009122)
                   Aplasia/Hypoplasia involving bones of the thorax(HPO:0006711)
                      Aplasia/Hypoplasia of the ribs(HPO:0006712)
                         Missing ribs(HPO:0000921)
                            11 pairs of ribs(HPO:0000878)
                Abnormality of the thorax(HPO:0000765)
                   Abnormality of the rib cage(HPO:0001547)
                      Abnormality of the ribs(HPO:0000772)
                         Aplasia/Hypoplasia of the ribs(HPO:0006712)
                            Missing ribs(HPO:0000921)
                               11 pairs of ribs(HPO:0000878)
                   Aplasia/Hypoplasia involving bones of the thorax(HPO:0006711)
                      Aplasia/Hypoplasia of the ribs(HPO:0006712)
                         Missing ribs(HPO:0000921)
                            11 pairs of ribs(HPO:0000878)
MedDRA:
Database Frequency: 19 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
Atelosteogenesis type I (Orphanet:1190)
Blackfan-Diamond anemia (Orphanet:124)
CAMPOMELIC DYSPLASIA (OMIM:114290)
Campomelic dysplasia (Orphanet:140)
Cerebro-costo-mandibular syndrome (Orphanet:1393)
Cloacal exstrophy (Orphanet:93929)
DIAMOND-BLACKFAN ANEMIA 1 (OMIM:105650)
Exstrophy-epispadias complex (Orphanet:322)
Greenberg dysplasia (Orphanet:1426)
Holoprosencephaly - postaxial polydactyly (Orphanet:2166)
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy (Orphanet:2958)
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I (OMIM:210710)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
SECKEL SYNDROME 1 (OMIM:210600)
Seckel syndrome (Orphanet:808)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Spondylometaphyseal dysplasia, Sedaghatian type (Orphanet:93317)
X-linked dominant chondrodysplasia, Chassaing-Lacombe type (Orphanet:163966)