Hypoplastic pelvis

Symptom Information:

Symptom ID: HPO:0008839
Synonyms:
Hypoplastic pelvic bones [HPO:0008839]
Small pelvis [HPO:0008839]
Hypoplastic pelvic bones [OMIM:Hypoplastic pelvic bones]
Hypoplastic pelvis [OMIM:Hypoplastic pelvis]
Small pelvis [OMIM:Small pelvis]
Quality:
Cross references:
OMIM: "Hypoplastic pelvic bones" [OMIM:Hypoplastic pelvic bones]
OMIM: "Hypoplastic pelvis" [OMIM:Hypoplastic pelvis]
OMIM: "Small pelvis" [OMIM:Small pelvis]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia involving the pelvis
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 pelvic girdle bone morphology(HPO:0002644)
                   Aplasia/Hypoplasia involving the pelvis(HPO:0009103)
                      Hypoplastic pelvis(HPO:0008839)
MedDRA:
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

3M syndrome (Orphanet:2616)
CHILD syndrome (Orphanet:139)
COCKAYNE SYNDROME A (OMIM:216400)
Cockayne syndrome (Orphanet:191)
Craniofaciofrontodigital syndrome (Orphanet:363705)
DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED (OMIM:304950)
FACIOCARDIOMELIC SYNDROME (OMIM:612731)
Fuhrmann syndrome (Orphanet:2854)
Jeune syndrome (Orphanet:474)
Kniest dysplasia (Orphanet:485)
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL (OMIM:602613)
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome (Orphanet:314394)
Short-rib thoracic dysplasia 1 with or without polydactyly (OMIM:208500)
Short-rib thoracic dysplasia 13 with or without polydactyly (OMIM:616300)
Spondylometaphyseal dysplasia, Schmidt type (Orphanet:93316)
THREE M SYNDROME 1 (OMIM:273750)
Tetraamelia - multiple malformations (Orphanet:3301)
Thoracolaryngopelvic dysplasia (Orphanet:3317)