| Rank (Similarity) |
PMID (PMCID) |
|
|---|---|---|
| 1 (45.7%) |
28193932 |
Localized Scleroderma (case Report of 23 Cases). Reddy BS, Singh G. Indian J Dermatol Venereol Leprol. 1982;48(5):276-281. |
| Hemiatrophy | ||
| 1 (45.7%) |
24860754 (4030347) |
Pansclerotic morphea: A male child with hemiatrophy of lower limb. Dasgupta MK, Patra C, Sarkar S, Das S. Indian Dermatol Online J. 2014;5(2):170-2. |
| Morphea Hemiatrophy | ||
| 1 (45.7%) |
11922240 |
Linear scleroderma and autoimmune hemolytic anaemia. Wanchu A, Sud A, Bambery P. J Assoc Physicians India. 2002;50:441-2. |
| Hemiatrophy | ||
| Adult Females Homo sapiens Mixed Connective Tissue Disease | ||
| 1 (45.7%) |
10768634 |
Hemimasticatory spasm associated with localized scleroderma and facial hemiatrophy. Kim HJ, Jeon BS, Lee KW. Arch Neurol. 2000;57(4):576-80. |
| Hemiatrophy | ||
| Action Potentials Adult Electromyography Facial Hemiatrophy Females Homo sapiens Hypertrophy Magnetic Resonance Imaging Reaction Time Reflex, Abnormal Trismus | ||
| 1 (45.7%) |
7271540 |
Myopathy associated with sclerodermal facial hemiatrophy. Schwartz RA, Tedesco AS, Stern LZ, Kaminska AM, Haraldsen JM, Grekin DA. Arch Neurol. 1981;38(9):592-4. |
| Myopathy Hemiatrophy | ||
| Adult Facial Hemiatrophy Females Homo sapiens Myopathy Skin | ||
| 1 (45.7%) |
3985735 |
Total hemiatrophy. Association with localized scleroderma, Schonlein-Henoch nephritis, and paroxysmal nocturnal hemoglobinuria. Kuto F, Sakaguchi T, Horasawa Y, Hayashi M, Hirasawa Y, Tokuhiro H. Arch Intern Med. 1985;145(4):731-3. |
| Nephritis Hemiatrophy | ||
| Adult Facial Hemiatrophy Females Glomerulonephritis Hemoglobinuria, Paroxysmal Henoch-Schoenlein Purpura Homo sapiens | ||
| 1 (45.7%) |
2930126 |
["Saber-cut" scleroderma and Parry-Romberg facial hemiatrophy. Nosologic problems. Neurologic complications]. Klene C, Massicot P, Ferriere-Fontan I, Sarlangue J, Fontan D, Guillard JM. Ann Pediatr (Paris). 1989;36(2):123-5. |
| Hypothyroidism Hemiatrophy | ||
| Brain Child Child, Preschool Epilepsy Facial Hemiatrophy Females Homo sapiens Systemic Scleroderma | ||
| 1 (45.7%) |
2707287 |
Progressive hemifacial atrophy with localized scleroderma. Tan E, Kurkcuoglu N, Atalag M, Gokoz A, Zileli T. Eur Neurol. 1989;29(1):15-7. |
| Hemiatrophy | ||
| Adult Facial Hemiatrophy Facial Muscles Females Homo sapiens X-Ray Computed Tomography | ||
| 1 (45.7%) |
1589383 |
Localized scleroderma and hemiatrophy in association with antibodies to double-stranded DNA. Adebajo AO, Crisp AJ, Nicholls A, Hazleman BL. Postgrad Med J. 1992;68(797):216-8. |
| Hemiatrophy | ||
| Antibodies, Antinuclear Females Foot Ulcer Homo sapiens Male Middle Aged | ||
| 1 (45.7%) |
1485755 |
[Facial hemiatrophy, homolateral cervical linear scleroderma and thyroid disease]. Claudy AL, Segault D, Rousset H, Moulin G. Ann Dermatol Venereol. 1992;119(8):543-5. |
| Hypothyroidism Hemiatrophy | ||
| Facial Dermatoses Facial Hemiatrophy Females Homo sapiens Hypothyroidism Middle Aged Neck |
Total: 16
| HPO ID | Term | Frequency |
|---|---|---|
| HP:0000953 | Hyperpigmentation of the skin | Very frequent (99-80%) |
| HP:0001010 | Hypopigmentation of the skin | Very frequent (99-80%) |
| HP:0001073 | Cigarette-paper scars | Very frequent (99-80%) |
| HP:0004334 | Dermal atrophy | Very frequent (99-80%) |
| HP:0030053 | Stiff skin | Very frequent (99-80%) |
| HP:0003202 | Skeletal muscle atrophy | Frequent (79-30%) |
| HP:0001171 | Split hand | Occasional (29-5%) |
| HP:0001371 | Flexion contracture | Occasional (29-5%) |
| HP:0002829 | Arthralgia | Occasional (29-5%) |
| HP:0003326 | Myalgia | Occasional (29-5%) |
| HP:0004552 | Scarring alopecia of scalp | Occasional (29-5%) |
| HP:0005830 | Flexion contracture of toe | Occasional (29-5%) |
| HP:0100556 | Hemiatrophy | Occasional (29-5%) |
| HP:0100557 | Hemiatrophy of lower limb | Occasional (29-5%) |
| HP:0100558 | Hemiatrophy of upper limb | Occasional (29-5%) |
| HP:0100578 | Lipoatrophy | Occasional (29-5%) |
Total: 40
| HPO ID | Term | # of case reports |
|---|---|---|
| HP:0012344 | Morphea | 63 |
| HP:0100556 | Hemiatrophy | 6 |
| HP:0001045 | Vitiligo | 5 |
| HP:0001250 | Seizures | 3 |
| HP:0001873 | Thrombocytopenia | 3 |
| HP:0000979 | Purpura | 2 |
| HP:0001269 | Hemiparesis | 2 |
| HP:0002860 | Squamous cell carcinoma | 2 |
| HP:0003198 | Myopathy | 2 |
| HP:0100578 | Lipoatrophy | 2 |
| HP:0000093 | Proteinuria | 1 |
| HP:0000123 | Nephritis | 1 |
| HP:0000790 | Hematuria | 1 |
| HP:0000821 | Hypothyroidism | 1 |
| HP:0000982 | Palmoplantar keratoderma | 1 |
| HP:0001271 | Polyneuropathy | 1 |
| HP:0001324 | Muscle weakness | 1 |
| HP:0001638 | Cardiomyopathy | 1 |
| HP:0001880 | Eosinophilia | 1 |
| HP:0002059 | Cerebral atrophy | 1 |
| HP:0002099 | Asthma | 1 |
| HP:0002716 | Lymphadenopathy | 1 |
| HP:0002754 | Osteomyelitis | 1 |
| HP:0002797 | Osteolysis | 1 |
| HP:0003095 | Septic arthritis | 1 |
| HP:0003394 | Muscle spasm | 1 |
| HP:0005293 | Venous insufficiency | 1 |
| HP:0009071 | Inflammatory myopathy | 1 |
| HP:0011099 | Spastic hemiparesis | 1 |
| HP:0011838 | Sclerodactyly | 1 |
| HP:0011946 | Bronchiolitis obliterans | 1 |
| HP:0012490 | Panniculitis | 1 |
| HP:0012733 | Macule | 1 |
| HP:0030816 | Gingival recession | 1 |
| HP:0032245 | Abnormal metabolism | 1 |
| HP:0032252 | Granuloma | 1 |
| HP:0100537 | Fasciitis | 1 |
| HP:0100543 | Cognitive impairment | 1 |
| HP:0100614 | Myositis | 1 |
| HP:0100646 | Thyroiditis | 1 |
Total: 0
| Gene Symbol | Gene Name | Entrez Gene ID |
|---|