Abnormality of the hand

Symptom Information:

Symptom ID: HPO:0001155
Synonyms:
Hand anomalies [HPO:0001155]
Hand deformities [HPO:0001155]
Hand anomaly [Orphanet:20000]
Hand anomalies [OMIM:Hand anomalies]
Hand deformities [OMIM:Hand deformities]
Anomalies of hands [Orphanet:20000]
Hand deformities (61%) [OMIM:Hand deformities (61%)]
Hand deformity [OMIM:Hand deformity]
Hand deformity [MedDRA:10061194]
Quality:
Cross references:
Orphanet:20000 "Anomalies of hands" [Orphanet:20000]
OMIM: "Hand anomalies" [OMIM:Hand anomalies]
OMIM: "Hand deformities" [OMIM:Hand deformities]
OMIM: "Hand deformities (61%)" [OMIM:Hand deformities (61%)]
OMIM: "Hand deformity" [OMIM:Hand deformity]
Is a (Direct Parents):
MedDRA Extremity deformities
Orphanet Upper limb segmental anomalies
HPO         Abnormality of the upper limb
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)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue deformities (incl intervertebral disc disorders)(MedDRA:10028377)
       Extremity deformities(MedDRA:10012139)
          Abnormality of the hand(HPO:0001155)
Database Frequency: 54 / 7739
Resource:

All diseases associated with this symptom:

3q13 microdeletion syndrome (Orphanet:1621)
Aarskog-Scott syndrome (Orphanet:915)
Alström syndrome (Orphanet:64)
Blackfan-Diamond anemia (Orphanet:124)
Bone dysplasia, lethal Holmgren type (Orphanet:1842)
Cataract - intellectual deficit - hypogonadism (Orphanet:1387)
Charcot-Marie-Tooth disease type 4D (Orphanet:99950)
Charcot-Marie-Tooth disease type 4G (Orphanet:99953)
Cleft palate - large ears - small head (Orphanet:2013)
Cohen syndrome (Orphanet:193)
Craniofacial conodysplasia (Orphanet:85168)
De Barsy syndrome (Orphanet:2962)
Dermatoosteolysis, Kirghizian type (Orphanet:1657)
Dermochondrocorneal dystrophy (Orphanet:79149)
Distal monosomy 13q (Orphanet:1590)
Dystrophic epidermolysis bullosa (Orphanet:303)
Ectodermal dysplasia syndrome (Orphanet:79373)
Embryonary disorganization syndrome (Orphanet:1664)
Episodic ataxia type 1 (Orphanet:37612)
FIBULAR APLASIA, TIBIAL CAMPOMELIA, AND OLIGOSYNDACTYLY SYNDROME (OMIM:246570)
Fabry disease (Orphanet:324)
Focal dermal hypoplasia (Orphanet:2092)
Giant axonal neuropathy (Orphanet:643)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
Hallermann-Streiff syndrome (Orphanet:2108)
Hereditary sensory and autonomic neuropathy with spastic paraplegia (Orphanet:139578)
Ichthyosis - oral and digital anomalies (Orphanet:2272)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Incontinentia pigmenti (Orphanet:464)
Laurence-Moon syndrome (Orphanet:2377)
MICROCEPHALY-MICROMELIA SYNDROME (OMIM:251230)
MUCOLIPIDOSIS III GAMMA (OMIM:252605)
Mesomelia-synostoses syndrome (Orphanet:2496)
Moebius syndrome (Orphanet:570)
Mosaic trisomy 15 (Orphanet:1706)
Mucopolysaccharidosis type 2 (Orphanet:580)
Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia (Orphanet:166029)
Nasu-Hakola disease (Orphanet:2770)
Navajo neurohepatopathy (Orphanet:255229)
Oculoosteocutaneous syndrome (Orphanet:2713)
PEHO syndrome (Orphanet:2836)
Poland syndrome (Orphanet:2911)
Progressive pseudorheumatoid arthropathy of childhood (Orphanet:1159)
Rhombencephalosynapsis (Orphanet:59315)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
Sillence syndrome (Orphanet:3168)
Stern-Lubinsky-Durrie syndrome (Orphanet:3194)
Thiemann disease, familial form (Orphanet:3314)
Tricho-retino-dento-digital syndrome (Orphanet:1264)
VAN MALDERGEM SYNDROME 1 (OMIM:601390)
VAN MALDERGEM SYNDROME 2 (OMIM:615546)
VELOCARDIOFACIAL SYNDROME (OMIM:192430)
WIDOW'S PEAK SYNDROME (OMIM:314570)
Wolf-Hirschhorn syndrome (Orphanet:280)