Absent ulna

Symptom Information:

Symptom ID: HPO:0003982
Synonyms:
Absent ossification/absent ulna [HPO:0003982]
ABSENT ULNAE [HPO:0003982]
Aplasia of the ulna [HPO:0003982]
Ulna absence [Orphanet:19300]
Congenital absence of ulna [HPO:0003982]
Congenital absence of ulna (disorder) [Orphanet:19300]
Congenital absence of ulna [Orphanet:19300]
Absent ulna [OMIM:Absent ulna]
Absent ulnae [OMIM:Absent ulnae]
Ulnar/cubital anomaly/absence/agenesis/hypoplasia/abnormal ulnar/cubital ray [Orphanet:19300]
Quality:
Cross references:
HPO:0006495 "Aplasia/Hypoplasia of the ulna" [Orphanet:19300]
Orphanet:19300 "Ulnar/cubital anomaly/absence/agenesis/hypoplasia/abnormal ulnar/cubital ray" [Orphanet:19300]
OMIM: "Absent ulna" [OMIM:Absent ulna]
OMIM: "Absent ulnae" [OMIM:Absent ulnae]
UMLS:C0431848 "Congenital absence of ulna" [Orphanet:19300]
Is a (Direct Parents):
HPO         Aplasia involving forearm bones
Orphanet Abnormality of the ulna
HPO         Absent forearm bone
HPO         Aplasia/Hypoplasia of the ulna
Orphanet Upper limb segmental anomalies
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)
                   Absent forearm bone(HPO:0003953)
                      Absent ulna(HPO:0003982)
             Aplasia/hypoplasia involving the skeleton(HPO:0009115)
                Aplasia/hypoplasia of the extremities(HPO:0009815)
                   Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                      Aplasia/hypoplasia involving forearm bones(HPO:0006503)
                         Aplasia/Hypoplasia of the ulna(HPO:0006495)
                            Absent ulna(HPO:0003982)
                         Aplasia involving forearm bones(HPO:0009822)
                            Absent ulna(HPO:0003982)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Aplasia/hypoplasia of the extremities(HPO:0009815)
                      Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                         Aplasia/hypoplasia involving forearm bones(HPO:0006503)
                            Aplasia/Hypoplasia of the ulna(HPO:0006495)
                               Absent ulna(HPO:0003982)
                            Aplasia involving forearm bones(HPO:0009822)
                               Absent ulna(HPO:0003982)
                   Abnormality of the upper limb(HPO:0002817)
                      Abnormality of the forearm(HPO:0002973)
                         Absent forearm bone(HPO:0003953)
                            Absent ulna(HPO:0003982)
                         Abnormality of the ulna(HPO:0002997)
                            Aplasia/Hypoplasia of the ulna(HPO:0006495)
                               Absent ulna(HPO:0003982)
                         Aplasia/hypoplasia involving forearm bones(HPO:0006503)
                            Aplasia/Hypoplasia of the ulna(HPO:0006495)
                               Absent ulna(HPO:0003982)
                            Aplasia involving forearm bones(HPO:0009822)
                               Absent ulna(HPO:0003982)
                      Aplasia/hypoplasia involving bones of the upper limbs(HPO:0006496)
                         Aplasia/hypoplasia involving forearm bones(HPO:0006503)
                            Aplasia/Hypoplasia of the ulna(HPO:0006495)
                               Absent ulna(HPO:0003982)
                            Aplasia involving forearm bones(HPO:0009822)
                               Absent ulna(HPO:0003982)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Acheiropodia (Orphanet:931)
Gollop-Wolfgang complex (Orphanet:1986)
Phocomelia, Schinzel type (Orphanet:2879)
SC PHOCOMELIA SYNDROME (OMIM:269000)
ULNAR AGENESIS AND ENDOCARDIAL FIBROELASTOSIS (OMIM:276822)
Ulbright-Hodes syndrome (Orphanet:3404)
Ulnar-mammary syndrome (Orphanet:3138)