Abnormality of the hand
Symptom Information:
| Symptom ID: | HPO:0001155 | |||||||||
| Synonyms: |
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| Is a (Direct Parents): |
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| 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) |
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| 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) |