Micropenis
Symptom Information:
Symptom ID: | HPO:0000054 | |||||||||||||||||
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 genitourinary system(HPO:0000119) Abnormality of the genital system(HPO:0000078) Abnormal genital system morphology(HPO:0012243) Abnormal external genitalia(HPO:0000811) External genital hypoplasia(HPO:0003241) Hypoplastic male external genitalia(HPO:0000050) Hypoplasia of penis(HPO:0008736) Micropenis(HPO:0000054) Abnormality of male external genitalia(HPO:0000032) Abnormality of the penis(HPO:0000036) Hypoplasia of penis(HPO:0008736) Micropenis(HPO:0000054) Hypoplastic male external genitalia(HPO:0000050) Hypoplasia of penis(HPO:0008736) Micropenis(HPO:0000054) Abnormality of the male genitalia(HPO:0010461) Abnormality of male external genitalia(HPO:0000032) Abnormality of the penis(HPO:0000036) Hypoplasia of penis(HPO:0008736) Micropenis(HPO:0000054) Hypoplastic male external genitalia(HPO:0000050) Hypoplasia of penis(HPO:0008736) Micropenis(HPO:0000054) MedDRA: Reproductive system and breast disorders(MedDRA:10038604) Penile and scrotal disorders (excl infections and inflammations)(MedDRA:10013355) Penile disorders NEC (excl erection and ejaculation)(MedDRA:10034304) Micropenis(HPO:0000054) |
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Database Frequency: | 257 / 7739 | |||||||||||||||||
Resource: |
All diseases associated with this symptom:
15q24 microdeletion syndrome | (Orphanet:94065) |
17p13.3 microduplication syndrome | (Orphanet:217385) |
1p36 deletion syndrome | (Orphanet:1606) |
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
2q23.1 microdeletion syndrome | (Orphanet:228402) |
3C syndrome | (Orphanet:7) |
3MC SYNDROME 3 | (OMIM:248340) |
3q13 microdeletion syndrome | (Orphanet:1621) |
46,XX ovotesticular disorder of sex development | (Orphanet:2138) |
46,XX testicular disorder of sex development | (Orphanet:393) |
46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency | (Orphanet:753) |
46,XY partial gonadal dysgenesis | (Orphanet:251510) |
48,XXXY syndrome | (Orphanet:96263) |
48,XXYY syndrome | (Orphanet:10) |
49,XXXXY syndrome | (Orphanet:96264) |
8p11.2 deletion syndrome | (Orphanet:251066) |
8q21.11 microdeletion syndrome | (Orphanet:284160) |
8q22.1 microdeletion syndrome | (Orphanet:178303) |
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS | (OMIM:201750) |
Ablepharon macrostomia syndrome | (Orphanet:920) |
Acro-cardio-facial syndrome | (Orphanet:2008) |
Acrocallosal syndrome | (Orphanet:36) |
Agnathia - holoprosencephaly - situs inversus | (Orphanet:990) |
Alopecia - intellectual deficit - hypergonadotropic hypogonadism | (Orphanet:1014) |
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 | (Orphanet:98791) |
Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
Anophthalmia/microphthalmia - esophageal atresia | (Orphanet:77298) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal dominant omodysplasia | (Orphanet:93328) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Autosomal recessive amelia | (Orphanet:1027) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
BARAITSER-WINTER SYNDROME 1 | (OMIM:243310) |
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA | (OMIM:609945) |
Baraitser-Winter syndrome | (Orphanet:2995) |
Bardet-Biedl syndrome | (Orphanet:110) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 8 | (OMIM:615985) |
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 | (Orphanet:231117) |
Bladder exstrophy | (Orphanet:93930) |
Borjeson-Forssman-Lehmann syndrome | (Orphanet:127) |
Brachydactyly - nystagmus - cerebellar ataxia | (Orphanet:1246) |
Brachydactyly type B | (Orphanet:93383) |
Brachytelephalangy - dysmorphism - Kallmann syndrome | (Orphanet:1295) |
CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III | (OMIM:611929) |
CARPENTER SYNDROME 2 | (OMIM:614976) |
CEREBROOCULOFACIOSKELETAL SYNDROME 2 | (OMIM:610756) |
CHARGE syndrome | (Orphanet:138) |
COCKAYNE SYNDROME A | (OMIM:216400) |
COCKAYNE SYNDROME B | (OMIM:133540) |
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG | (OMIM:218649) |
CULLER-JONES SYNDROME | (OMIM:615849) |
Cabezas syndrome | (Orphanet:85293) |
Cardiocranial syndrome, Pfeiffer type | (Orphanet:2872) |
Carpenter-Waziri syndrome | (Orphanet:93973) |
Cataract - intellectual deficit - anal atresia - urinary defects | (Orphanet:1381) |
Cataract - intellectual deficit - hypogonadism | (Orphanet:1387) |
Caudal appendage - deafness | (Orphanet:1123) |
Cerebro-oculo-nasal syndrome | (Orphanet:66625) |
Chudley-Lowry-Hoar syndrome | (Orphanet:93971) |
Cloacal exstrophy | (Orphanet:93929) |
Cockayne syndrome | (Orphanet:191) |
Congenital osteogenesis imperfecta - microcephaly - cataracts | (Orphanet:2772) |
Cornelia de Lange syndrome | (Orphanet:199) |
Crandall syndrome | (Orphanet:202) |
Crane-Heise syndrome | (Orphanet:1512) |
Craniofacial-ulnar-renal syndrome | (Orphanet:293843) |
Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis | (Orphanet:171839) |
Crossed polysyndactyly | (Orphanet:2935) |
Currarino triad | (Orphanet:1552) |
Deafness - intellectual deficit, Martin-Probst type | (Orphanet:85321) |
Disorder of sex development - intellectual deficit | (Orphanet:2983) |
Distal monosomy 10p | (Orphanet:1580) |
Distal monosomy 10q | (Orphanet:96148) |
Distal monosomy 15q | (Orphanet:1596) |
Distal monosomy 7q36 | (Orphanet:1636) |
Distal trisomy 18q | (Orphanet:1716) |
Dysmorphism - short stature - deafness - disorder of sex development | (Orphanet:2282) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 | (OMIM:129900) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 | (OMIM:604292) |
EEC syndrome | (Orphanet:1896) |
Ear-patella-short stature syndrome | (Orphanet:2554) |
Ectodermal dysplasia - intellectual deficit - central nervous system malformation | (Orphanet:1812) |
Ectodermal dysplasia, Berlin type | (Orphanet:1816) |
Emanuel syndrome | (Orphanet:96170) |
Endocrine-cerebro-osteodysplasia syndrome | (Orphanet:199332) |
Endomyocardial fibroelastosis | (Orphanet:2022) |
Exstrophy-epispadias complex | (Orphanet:322) |
FANCONI ANEMIA, COMPLEMENTATION GROUP L | (OMIM:614083) |
Familial adrenal hypoplasia with absent pituitary luteinizing hormone | (Orphanet:95700) |
Femoral-facial syndrome | (Orphanet:1988) |
Fibulo-ulnar hypoplasia - renal anomalies | (Orphanet:2256) |
Floating-Harbor syndrome | (Orphanet:2044) |
Fraser syndrome | (Orphanet:2052) |
Gemignani syndrome | (Orphanet:2074) |
Genitopatellar syndrome | (Orphanet:85201) |
Growth hormone insensitivity syndrome | (Orphanet:181393) |
HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION | (OMIM:613870) |
HOLOPROSENCEPHALY 1 | (OMIM:236100) |
HOLOPROSENCEPHALY 9 | (OMIM:610829) |
HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS | (OMIM:610680) |
HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITALABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES | (OMIM:614684) |
HYPOGONADISM, MALEHYPOGONADISM AND TESTICULAR ATROPHY, INCLUDED | (OMIM:241100) |
HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA | (OMIM:308700) |
HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA | (OMIM:614840) |
HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA | (OMIM:614841) |
HYPOGONADOTROPIC HYPOGONADISM 15 WITH OR WITHOUT ANOSMIA | (OMIM:614880) |
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA | (OMIM:614897) |
HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA | (OMIM:616030) |
HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA | (OMIM:228300) |
HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA | (OMIM:244200) |
HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA | (OMIM:610628) |
HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA | (OMIM:614837) |
HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED | (OMIM:241800) |
Hand-foot-genital syndrome | (Orphanet:2438) |
Hartsfield-Bixler-Demyer syndrome | (Orphanet:2117) |
Holmes-Gang syndrome | (Orphanet:93970) |
Holoprosencephaly | (Orphanet:2162) |
Holoprosencephaly - postaxial polydactyly | (Orphanet:2166) |
Hydrocephalus - obesity - hypogonadism | (Orphanet:2183) |
Hypogonadotropic hypogonadism - frontoparietal alopecia | (Orphanet:2230) |
Hyposmia - nasal and ocular hypoplasia - hypogonadotropic hypogonadism | (Orphanet:2250) |
IMAGe syndrome | (Orphanet:85173) |
IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES | (OMIM:615966) |
Intellectual deficit - myopathy - short stature - endocrine defect | (Orphanet:3068) |
Intellectual deficit - polydactyly - uncombable hair | (Orphanet:3082) |
Intellectual deficit, X-linked - short stature - obesity | (Orphanet:3055) |
Intellectual deficit, X-linked, Nascimento type | (Orphanet:163956) |
Intellectual deficit, X-linked, Vitale type | (Orphanet:85289) |
Johanson-Blizzard syndrome | (Orphanet:2315) |
Joubert syndrome 15 | (OMIM:614464) |
Joubert syndrome 2 | (OMIM:608091) |
Juberg-Marsidi syndrome | (Orphanet:93972) |
KABUKI SYNDROME 1 | (OMIM:147920) |
KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA | (OMIM:308750) |
Kabuki syndrome | (Orphanet:2322) |
Kallmann syndrome | (Orphanet:478) |
Kallmann syndrome - heart disease | (Orphanet:2326) |
Kapur-Toriello syndrome | (Orphanet:2328) |
Kenny-Caffey syndrome | (Orphanet:2333) |
Kleefstra syndrome | (Orphanet:261494) |
Kleefstra syndrome due to 9q34 microdeletion | (Orphanet:96147) |
LEOPARD SYNDROME 1 | (OMIM:151100) |
LIG4 syndrome | (Orphanet:99812) |
Laron syndrome | (Orphanet:633) |
Lathosterolosis | (Orphanet:46059) |
Laurence-Moon syndrome | (Orphanet:2377) |
Lethal hemolytic anemia - genital anomalies | (Orphanet:1046) |
Lissencephaly type 1 due to doublecortin gene mutation | (Orphanet:2148) |
MEHMO syndrome | (Orphanet:85282) |
MEIER-GORLIN SYNDROME 1 | (OMIM:224690) |
MEIER-GORLIN SYNDROME 5 | (OMIM:613805) |
MENTAL RETARDATION, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENISSYNDROME | (OMIM:610156) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I | (OMIM:210710) |
MICROPHTHALMIA, SYNDROMIC 7 | (OMIM:309801) |
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 | (OMIM:257300) |
MOVED TO 614732 | (OMIM:300290) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 2 | (OMIM:613156) |
Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies | (Orphanet:2234) |
Marden-Walker syndrome | (Orphanet:2461) |
Maternal hyperthermia induced birth defects | (Orphanet:2216) |
Meacham syndrome | (Orphanet:3097) |
Micro syndrome | (Orphanet:2510) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Microcephaly - seizures - intellectual deficit - heart disease | (Orphanet:2519) |
Microphthalmia - microtia - fetal akinesia | (Orphanet:2547) |
Microphthalmia with brain and digit anomalies | (Orphanet:139471) |
Mikati-Najjar-Sahli syndrome | (Orphanet:2558) |
Moebius syndrome | (Orphanet:570) |
Monosomy 18p | (Orphanet:1598) |
Monosomy 18q | (Orphanet:1600) |
Monosomy 9p | (Orphanet:261112) |
Mosaic trisomy 14 | (Orphanet:1703) |
Mosaic trisomy 9 | (Orphanet:99776) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
Mullerian derivatives - lymphangiectasia - polydactyly | (Orphanet:1655) |
Mullerian duct anomalies - limb anomalies | (Orphanet:2491) |
Neuroectodermal syndrome, Johnson type | (Orphanet:2316) |
Non-rhizomelic chondrodysplasia punctata | (Orphanet:176) |
Noonan syndrome with multiple lentigines | (Orphanet:500) |
Normosmic congenital hypogonadotropic hypogonadism | (Orphanet:432) |
OROFACIODIGITAL SYNDROME XIV | (OMIM:615948) |
Obesity due to congenital leptin deficiency | (Orphanet:66628) |
Omodysplasia | (Orphanet:2733) |
Osteocraniostenosis | (Orphanet:2763) |
PELVIS syndrome | (Orphanet:83628) |
PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY | (OMIM:602342) |
Pallister-Hall syndrome | (Orphanet:672) |
Partial androgen insensitivity syndrome | (Orphanet:90797) |
Perlman syndrome | (Orphanet:2849) |
Phocomelia, Schinzel type | (Orphanet:2879) |
Pierson syndrome | (Orphanet:2670) |
Pitt-Hopkins syndrome | (Orphanet:2896) |
Pituitary stalk interruption syndrome | (Orphanet:95496) |
Pontocerebellar hypoplasia type 7 | (Orphanet:284339) |
Postaxial acrofacial dysostosis | (Orphanet:246) |
Potocki-Shaffer syndrome | (Orphanet:52022) |
Prader-Willi syndrome | (Orphanet:739) |
Prominent glabella - microcephaly - hypogenitalism | (Orphanet:2083) |
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2 | (OMIM:616331) |
Renier-Gabreels-Jasper syndrome | (Orphanet:93975) |
Retinitis pigmentosa | (Orphanet:791) |
Retinohepatoendocrinologic syndrome | (Orphanet:3087) |
Rudiger syndrome | (Orphanet:3118) |
SCARF syndrome | (Orphanet:3134) |
SCHAAF-YANG SYNDROME | (OMIM:615547) |
SENER SYNDROME | (OMIM:606156) |
SHORT RIB-POLYDACTYLY SYNDROME, TYPE IIB | (OMIM:615087) |
SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION | (OMIM:612447) |
STT3B-CDG | (Orphanet:370924) |
Sanjad-Sakati syndrome | (Orphanet:2323) |
Schinzel-Giedion syndrome | (Orphanet:798) |
Septo-optic dysplasia | (Orphanet:3157) |
Short rib-polydactyly syndrome, Majewski type | (Orphanet:93269) |
Short-rib thoracic dysplasia 3 with or without polydactyly | (OMIM:613091) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Simpson-Golabi-Behmel syndrome type 2 | (Orphanet:79022) |
Smith-Fineman-Myers syndrome | (Orphanet:93974) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Solitary median maxillary central incisor syndrome | (Orphanet:2286) |
Spondylocostal dysostosis - anal and genitourinary malformations | (Orphanet:94095) |
Sudden infant death - dysgenesis of the testes | (Orphanet:168593) |
Summitt syndrome | (Orphanet:3210) |
Syndromic X-linked intellectual deficit 7 | (Orphanet:85274) |
Syndromic X-linked intellectual deficit due to JARID1C mutation | (Orphanet:85279) |
Syndromic microphthalmia type 5 | (Orphanet:178364) |
TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE | (OMIM:615542) |
Tel Hashomer camptodactyly syndrome | (Orphanet:3292) |
Testicular regression syndrome | (Orphanet:983) |
Toriello-Carey syndrome | (Orphanet:3338) |
Townes-Brocks syndrome | (Orphanet:857) |
Treacher-Collins syndrome | (Orphanet:861) |
Triploidy | (Orphanet:3376) |
Trisomy 17p | (Orphanet:261290) |
Trisomy 5p | (Orphanet:1742) |
Trisomy 8q | (Orphanet:1752) |
Ulnar-mammary syndrome | (Orphanet:3138) |
Urban-Rogers-Meyer syndrome | (Orphanet:3409) |
VACTERL/VATER association | (Orphanet:887) |
VAN MALDERGEM SYNDROME 2 | (OMIM:615546) |
Van Regemorter-Pierquin-Vamos syndrome | (Orphanet:3419) |
Von Voss-Cherstvoy syndrome | (Orphanet:3439) |
WARBURG MICRO SYNDROME 2 | (OMIM:614225) |
WARBURG MICRO SYNDROME 3 | (OMIM:614222) |
WARBURG MICRO SYNDROME 4 | (OMIM:615663) |
Walker-Warburg syndrome | (Orphanet:899) |
Weaver syndrome | (Orphanet:3447) |
Williams syndrome | (Orphanet:904) |
Wilson-Turner syndrome | (Orphanet:3459) |
Woodhouse-Sakati syndrome | (Orphanet:3464) |
X-linked distal arthrogryposis multiplex congenita | (Orphanet:1145) |
X-linked intellectual deficit - cerebellar hypoplasia | (Orphanet:137831) |
X-linked intellectual deficit - hypotonic face | (Orphanet:73220) |
X-linked lissencephaly with abnormal genitalia | (Orphanet:452) |
Yunis-Varon syndrome | (Orphanet:3472) |