Abnormality of finger

Symptom Information:

Symptom ID: HPO:0001167
Synonyms:
Abnormalities of the fingers [HPO:0001167]
Abnormalities of the fingers (45%) [OMIM:Abnormalities of the fingers (45%)]
Quality:
Cross references:
OMIM: "Abnormalities of the fingers (45%)" [OMIM:Abnormalities of the fingers (45%)]
Is a (Direct Parents):
HPO         Abnormality of digit
HPO         Abnormality of the hand
HPO         Splayed fingers
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 finger(HPO:0001167)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of finger(HPO:0001167)
MedDRA:
Database Frequency: 29 / 7739
Resource:

All diseases associated with this symptom:

Acrofacial dysostosis, Catania type (Orphanet:1786)
Acromesomelic dysplasia, Hunter-Thomson type (Orphanet:968)
Adams-Oliver syndrome (Orphanet:974)
Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet:1154)
Bazex-Dupré-Christol syndrome (Orphanet:113)
Brachydactyly - arterial hypertension (Orphanet:1276)
CATARACT 5, MULTIPLE TYPES (OMIM:116800)
Chondrodysplasia - disorder of sex development (Orphanet:1422)
Cleidorhizomelic syndrome (Orphanet:1453)
Distal monosomy 17q (Orphanet:1597)
Epilepsy telangiectasia (Orphanet:1951)
Epiphyseal dysplasia - hearing loss - dysmorphism (Orphanet:1825)
Familial digital arthropathy-brachydactyly (Orphanet:85169)
Fanconi anemia (Orphanet:84)
Heart-hand syndrome type 3 (Orphanet:1342)
Histidinuria - renal tubular defect (Orphanet:2158)
Hurler syndrome (Orphanet:93473)
Leri pleonosteosis (Orphanet:2900)
Lethal faciocardiomelic dysplasia (Orphanet:1972)
Linear nevus sebaceus syndrome (Orphanet:2612)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Non-rhizomelic chondrodysplasia punctata (Orphanet:176)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 3 (Orphanet:2752)
Paraplegia - brachydactyly - cone-shaped epiphysis (Orphanet:2823)
Sclerosteosis (Orphanet:3152)
Skeletal dysplasia - epilepsy - short stature (Orphanet:1858)
Triphalangeal thumbs - brachyectrodactyly (Orphanet:2947)
Waardenburg syndrome type 3 (Orphanet:896)