Small hypothenar eminence

Symptom Information:

Symptom ID: HPO:0010487
Synonyms:
Hypoplasia of the hypothenar eminence [HPO:0010487]
Hypothenar hypoplasia [HPO:0010487]
Hypothenar hypoplasia [OMIM:Hypothenar hypoplasia]
Quality:
Cross references:
OMIM: "Hypothenar hypoplasia" [OMIM:Hypothenar hypoplasia]
Is a (Direct Parents):
HPO         Abnormality of the hypothenar eminence
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 upper limb(HPO:0002817)
                      Abnormality of the hand(HPO:0001155)
                         Abnormality of the musculature of the hand(HPO:0001421)
                            Abnormality of the hypothenar eminence(HPO:0010486)
                               Small hypothenar eminence(HPO:0010487)
                   Abnormality of the musculature of the limbs(HPO:0009127)
                      Abnormality of the musculature of the upper limbs(HPO:0001446)
                         Abnormality of the musculature of the hand(HPO:0001421)
                            Abnormality of the hypothenar eminence(HPO:0010486)
                               Small hypothenar eminence(HPO:0010487)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of the musculature of the limbs(HPO:0009127)
             Abnormality of the musculature of the upper limbs(HPO:0001446)
                Abnormality of the musculature of the hand(HPO:0001421)
                   Abnormality of the hypothenar eminence(HPO:0010486)
                      Small hypothenar eminence(HPO:0010487)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III (OMIM:611929)
DIAMOND-BLACKFAN ANEMIA 7 (OMIM:612562)
Symphalangism with multiple anomalies of hands and feet (Orphanet:3246)
Tel Hashomer camptodactyly syndrome (Orphanet:3292)