Osteolytic defects of the phalanges of the hand

Symptom Information:

Symptom ID: HPO:0009771
Synonyms:
Acro-osteolysis [HPO:0009771]
Acroosteolysis [HPO:0009771]
Acro-Osteolysis [HPO:0009771]
Acro-osteolysis [OMIM:Acro-osteolysis]
Acroosteolysis [OMIM:Acroosteolysis]
Quality:
Cross references:
OMIM: "Acro-osteolysis" [OMIM:Acro-osteolysis]
OMIM: "Acroosteolysis" [OMIM:Acroosteolysis]
UMLS:C0917990 "Acro-Osteolysis" [HPO:0009771]
Is a (Direct Parents):
HPO         Abnormality of phalanx of finger
HPO         Osteolytic defects of the hand bones
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)
                Osteolysis(HPO:0002797)
                   Osteolytic defects of the hand bones(HPO:0009699)
                      Osteolytic defects of the phalanges of the hand(HPO:0009771)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of finger(HPO:0001167)
                         Abnormality of phalanx of finger(HPO:0005918)
                            Osteolytic defects of the phalanges of the hand(HPO:0009771)
                   Abnormality of the upper limb(HPO:0002817)
                      Abnormality of the hand(HPO:0001155)
                         Osteolytic defects of the hand bones(HPO:0009699)
                            Osteolytic defects of the phalanges of the hand(HPO:0009771)
                         Abnormality of finger(HPO:0001167)
                            Abnormality of phalanx of finger(HPO:0005918)
                               Osteolytic defects of the phalanges of the hand(HPO:0009771)
MedDRA:
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

Acro-osteolysis-keloid-like lesions-premature aging syndrome (Orphanet:363665)
Acroosteolysis, dominant type (Orphanet:955)
Cranio-osteoarthropathy (Orphanet:1525)
Diffuse cutaneous systemic sclerosis (Orphanet:220393)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
HAJDU-CHENEY SYNDROME (OMIM:102500)
Haim-Munk syndrome (Orphanet:2342)
Hereditary sensory and autonomic neuropathy type 2 (Orphanet:970)
Limited cutaneous systemic sclerosis (Orphanet:220402)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA (OMIM:201300)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB (OMIM:613115)
NEUROPATHY, HEREDITARY SENSORY, TYPE IF (OMIM:615632)
Necrotizing encephalomyelopathy, subacute, of Leigh, adult (OMIM:161700)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
SATOYOSHI SYNDROME (OMIM:600705)
Singleton-Merten dysplasia (Orphanet:85191)
VAN BOGAERT-HOZAY SYNDROME (OMIM:277150)