Hypoplastic ischia

Symptom Information:

Symptom ID: HPO:0003175
Synonyms:
Hypoplastic ischial bones [HPO:0003175]
Hypoplastic ischii [HPO:0003175]
Hypoplastic ischium [HPO:0003175]
Hypoplastic ischia [OMIM:Hypoplastic ischia]
Hypoplastic ischial bones [OMIM:Hypoplastic ischial bones]
Hypoplastic ischii [OMIM:Hypoplastic ischii]
Hypoplastic ischium [OMIM:Hypoplastic ischium]
Quality:
Cross references:
OMIM: "Hypoplastic ischia" [OMIM:Hypoplastic ischia]
OMIM: "Hypoplastic ischial bones" [OMIM:Hypoplastic ischial bones]
OMIM: "Hypoplastic ischii" [OMIM:Hypoplastic ischii]
OMIM: "Hypoplastic ischium" [OMIM:Hypoplastic ischium]
Is a (Direct Parents):
HPO         Abnormality of the ischium
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 joint morphology(HPO:0001367)
                Abnormality of lower limb joint(HPO:0100491)
                   Abnormality of the hip bone(HPO:0003272)
                      Abnormality of the ischium(HPO:0003174)
                         Hypoplastic ischia(HPO:0003175)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the lower limb(HPO:0002814)
                      Abnormality of lower limb joint(HPO:0100491)
                         Abnormality of the hip bone(HPO:0003272)
                            Abnormality of the ischium(HPO:0003174)
                               Hypoplastic ischia(HPO:0003175)
                Abnormality of pelvic girdle bone morphology(HPO:0002644)
                   Abnormality of the hip bone(HPO:0003272)
                      Abnormality of the ischium(HPO:0003174)
                         Hypoplastic ischia(HPO:0003175)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Achondrogenesis (Orphanet:932)
Achondrogenesis type 1A (Orphanet:93299)
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED (OMIM:304950)
FIBROCHONDROGENESIS 2 (OMIM:614524)
Fibrochondrogenesis (Orphanet:2021)
Genitopatellar syndrome (Orphanet:85201)
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III (OMIM:210730)
Opsismodysplasia (Orphanet:2746)
Pelviscapular dysplasia (Orphanet:93333)
Platyspondylic dysplasia, Torrance type (Orphanet:85166)
SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE (OMIM:613320)