Split hand
Symptom Information:
Symptom ID: | HPO:0001171 | ||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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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) Split hand(HPO:0001171) Ectrodactyly(HPO:0100257) Split hand(HPO:0001171) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396) Musculoskeletal and connective tissue disorders of limbs congenital(MedDRA:10028381) Split hand(HPO:0001171) |
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Database Frequency: | 72 / 7739 | ||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ACRORENAL SYNDROME, AUTOSOMAL RECESSIVE | (OMIM:201310) |
ADULT syndrome | (Orphanet:978) |
ANONYCHIA-ECTRODACTYLY | (OMIM:106900) |
ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY | (OMIM:106990) |
Acro-cardio-facial syndrome | (Orphanet:2008) |
Acro-renal-mandibular syndrome | (Orphanet:958) |
Autosomal dominant Charcot-Marie-Tooth disease type 2E | (Orphanet:99939) |
Autosomal dominant Charcot-Marie-Tooth disease type 2F | (Orphanet:99940) |
Autosomal dominant Charcot-Marie-Tooth disease type 2K | (Orphanet:99944) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E | (Orphanet:93114) |
Autosomal recessive Charcot-Marie-Tooth disease with hoarseness | (Orphanet:101097) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A | (Orphanet:217055) |
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA | (OMIM:609945) |
BROWN-VIALETTO-VAN LAERE SYNDROME 2 | (OMIM:614707) |
Bifunctional enzyme deficiency | (Orphanet:300) |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE | (OMIM:607706) |
CHARGE syndrome | (Orphanet:138) |
CHROMOSOME 17p13.3, TELOMERIC, DUPLICATION SYNDROME | (OMIM:612576) |
Charcot-Marie-Tooth disease type 1A | (Orphanet:101081) |
Charcot-Marie-Tooth disease type 1B | (Orphanet:101082) |
Charcot-Marie-Tooth disease type 1E | (Orphanet:90658) |
Charcot-Marie-Tooth disease type 4A | (Orphanet:99948) |
Charcot-Marie-Tooth disease type 4B2 | (Orphanet:99956) |
Congenital cataracts - facial dysmorphism - neuropathy | (Orphanet:48431) |
Dejerine-Sottas syndrome | (Orphanet:64748) |
Dermatoosteolysis, Kirghizian type | (Orphanet:1657) |
Distal hereditary motor neuropathy, Jerash type | (Orphanet:139552) |
Distal limb deficiencies - micrognathia syndrome | (Orphanet:1307) |
Dystrophic epidermolysis bullosa | (Orphanet:303) |
ECTRODACTYLY AND ECTODERMAL DYSPLASIA WITHOUT CLEFT LIP/PALATE | (OMIM:129810) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 | (OMIM:604292) |
ECTRODACTYLY-CLEFT PALATE SYNDROME | (OMIM:129830) |
EEC syndrome | (Orphanet:1896) |
EEM syndrome | (Orphanet:1897) |
Ectrodactyly - polydactyly | (Orphanet:1892) |
Focal dermal hypoplasia | (Orphanet:2092) |
Gollop-Wolfgang complex | (Orphanet:1986) |
Hurler syndrome | (Orphanet:93473) |
Hypoglossia - hypodactyly | (Orphanet:989) |
Intellectual deficit - spasticity - ectrodactyly | (Orphanet:1891) |
Karsch-Neugebauer syndrome | (Orphanet:2329) |
Limb-mammary syndrome | (Orphanet:69085) |
Limited cutaneous systemic sclerosis | (Orphanet:220402) |
Localized scleroderma | (Orphanet:90289) |
MUCOLIPIDOSIS III ALPHA/BETA | (OMIM:252600) |
MUCOLIPIDOSIS III GAMMA | (OMIM:252605) |
MYOPATHY, DISTAL, 3 | (OMIM:610099) |
Moebius syndrome | (Orphanet:570) |
Mucolipidosis type 2 | (Orphanet:576) |
Mucolipidosis type 3 | (Orphanet:577) |
Mucopolysaccharidosis type 1 | (Orphanet:579) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Mucopolysaccharidosis type 6 | (Orphanet:583) |
Mullerian duct anomalies - limb anomalies | (Orphanet:2491) |
OPITZ-KAVEGGIA SYNDROME | (OMIM:305450) |
Patterson-Stevenson-Fontaine syndrome | (Orphanet:2439) |
Phocomelia - ectrodactyly - deafness - sinus arrhythmia | (Orphanet:2878) |
Phocomelia, Schinzel type | (Orphanet:2879) |
SPLIT-HAND AND SPLIT-FOOT WITH HYPODONTIA | (OMIM:183500) |
SPLIT-HAND/FOOT MALFORMATION 1 | (OMIM:183600) |
SPLIT-HAND/FOOT MALFORMATION 2 | (OMIM:313350) |
SPLIT-HAND/FOOT MALFORMATION 4 | (OMIM:605289) |
SPLIT-HAND/FOOT MALFORMATION 6 | (OMIM:225300) |
Scheie syndrome | (Orphanet:93474) |
Split hand - split foot - deafness | (Orphanet:71271) |
Split hand - urinary anomalies - spina bifida | (Orphanet:2437) |
Split hand-split foot malformation | (Orphanet:2440) |
Tetramelic monodactyly | (Orphanet:2564) |
Tibial aplasia - ectrodactyly | (Orphanet:3329) |
Torg-Winchester syndrome | (Orphanet:3460) |
Triphalangeal thumbs - brachyectrodactyly | (Orphanet:2947) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |