Aplasia/Hypoplasia of the palmar creases

Symptom Information:

Symptom ID: HPO:0010488
Synonyms:
Decreased Palmar Creases [Orphanet:20240]
Flat palm [Orphanet:20240]
Quality:
Cross references:
HPO:0006184 "Decreased palmar creases" [Orphanet:20240]
Orphanet:20240 "Flat palm" [Orphanet:20240]
Is a (Direct Parents):
HPO         Abnormality of the palmar creases
Orphanet Abnormality of the hand
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)
                Abnormal dermatoglyphics(HPO:0007477)
                   Abnormal palmar dermatoglyphics(HPO:0001018)
                      Abnormality of the palmar creases(HPO:0010490)
                         Aplasia/Hypoplasia of the palmar creases(HPO:0010488)
       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 palm(HPO:0100871)
                            Abnormal palmar dermatoglyphics(HPO:0001018)
                               Abnormality of the palmar creases(HPO:0010490)
                                  Aplasia/Hypoplasia of the palmar creases(HPO:0010488)
MedDRA:
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

Aase-Smith syndrome (Orphanet:916)
Acro-oto-ocular syndrome (Orphanet:2980)
Arthrogryposis multiplex congenita - whistling face (Orphanet:1150)
Charcot-Marie-Tooth disease (Orphanet:166)
Hand-foot-genital syndrome (Orphanet:2438)
Hereditary neuropathy with liability to pressure palsies (Orphanet:640)
Hypertelorism-microtia-facial clefting syndrome (Orphanet:2213)
Jacobsen syndrome (Orphanet:2308)
Marfanoid habitus - intellectual deficit, autosomal recessive (Orphanet:2463)
Say-Field-Coldwell syndrome (Orphanet:3133)
X-linked Charcot-Marie-Tooth disease type 1 (Orphanet:101075)
X-linked Charcot-Marie-Tooth disease type 2 (Orphanet:101076)
X-linked Charcot-Marie-Tooth disease type 3 (Orphanet:101077)
X-linked Charcot-Marie-Tooth disease type 4 (Orphanet:101078)
X-linked Charcot-Marie-Tooth disease type 5 (Orphanet:99014)