Prominent fingertip pads

Symptom Information:

Symptom ID: HPO:0001212
Synonyms:
Persistence of fingerpads [HPO:0001212]
Persistent fetal fingertip pads [HPO:0001212]
Prominent finger pads [HPO:0001212]
Persistence of fingerpads [OMIM:Persistence of fingerpads]
Persistent fetal fingertip pads [OMIM:Persistent fetal fingertip pads]
Prominent finger pads [OMIM:Prominent finger pads]
Prominent fingertip pads [OMIM:Prominent fingertip pads]
Quality:
Cross references:
OMIM: "Persistence of fingerpads" [OMIM:Persistence of fingerpads]
OMIM: "Persistent fetal fingertip pads" [OMIM:Persistent fetal fingertip pads]
OMIM: "Prominent finger pads" [OMIM:Prominent finger pads]
OMIM: "Prominent fingertip pads" [OMIM:Prominent fingertip pads]
Is a (Direct Parents):
HPO         Prominent digit pad
HPO         Abnormality of the fingertips
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Regional abnormality of skin(HPO:0011356)
                Prominent digit pad(HPO:0011298)
                   Prominent fingertip pads(HPO:0001212)
       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 the fingertips(HPO:0001211)
                               Prominent fingertip pads(HPO:0001212)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of finger(HPO:0001167)
                         Abnormality of the fingertips(HPO:0001211)
                            Prominent fingertip pads(HPO:0001212)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Fryns syndrome (Orphanet:2059)
HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVEFACIAL FEATURES (OMIM:609943)
KABUKI SYNDROME 1 (OMIM:147920)
KABUKI SYNDROME 2 (OMIM:300867)
Kabuki syndrome (Orphanet:2322)
Koolen-De Vries syndrome (Orphanet:96169)
Noonan syndrome (Orphanet:648)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
Velo-facial-skeletal syndrome (Orphanet:3424)
Weaver syndrome (Orphanet:3447)