Hypoplastic ilia

Symptom Information:

Symptom ID: HPO:0000946
Synonyms:
Short and small iliac bones [HPO:0000946]
Small iliac bones [HPO:0000946]
Hypoplastic ilia [OMIM:Hypoplastic ilia]
Short and small iliac bones [OMIM:Short and small iliac bones]
Small iliac bones [OMIM:Small iliac bones]
Quality:
Cross references:
OMIM: "Hypoplastic ilia" [OMIM:Hypoplastic ilia]
OMIM: "Short and small iliac bones" [OMIM:Short and small iliac bones]
OMIM: "Small iliac bones" [OMIM:Small iliac bones]
Is a (Direct Parents):
HPO         Abnormality of the ilium
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 lower limb(HPO:0002814)
                      Abnormality of lower limb joint(HPO:0100491)
                         Abnormality of the hip bone(HPO:0003272)
                            Abnormality of the ilium(HPO:0002867)
                               Hypoplastic ilia(HPO:0000946)
                Abnormality of pelvic girdle bone morphology(HPO:0002644)
                   Abnormality of the hip bone(HPO:0003272)
                      Abnormality of the ilium(HPO:0002867)
                         Hypoplastic ilia(HPO:0000946)
             Abnormal joint morphology(HPO:0001367)
                Abnormality of lower limb joint(HPO:0100491)
                   Abnormality of the hip bone(HPO:0003272)
                      Abnormality of the ilium(HPO:0002867)
                         Hypoplastic ilia(HPO:0000946)
MedDRA:
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

Achondrogenesis type 1B (Orphanet:93298)
Anauxetic dysplasia (Orphanet:93347)
Blackfan-Diamond anemia (Orphanet:124)
DIAMOND-BLACKFAN ANEMIA 1 (OMIM:105650)
FIBROCHONDROGENESIS 2 (OMIM:614524)
Hurler syndrome (Orphanet:93473)
Lethal Kniest-like dysplasia (Orphanet:2347)
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I (OMIM:210710)
Marshall syndrome (Orphanet:560)
Metaphyseal chondrodysplasia, Kaitila type (Orphanet:166038)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 2 (Orphanet:90652)
Pelvis-shoulder dysplasia (Orphanet:2839)
Pelviscapular dysplasia (Orphanet:93333)
Platyspondylic dysplasia, Torrance type (Orphanet:85166)
Severe achondroplasia - developmental delay - acanthosis nigricans (Orphanet:85165)
Spondylo-megaepiphyseal-metaphyseal dysplasia (Orphanet:228387)
THANATOPHORIC DYSPLASIA, TYPE II (OMIM:187601)
Thanatophoric dysplasia type 1 (Orphanet:1860)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)